Proprietary Name,NDC Package Code,Strength,Dosage Form,Route,Appl. No.,Labeler Name,Product NDC,Nonproprietary Name,Substance Name,Product Type Name,Start Marketing Date,End Marketing Date,Market Category,Package Description,Pharm Class,DEA,Sample Package,Listing Record Certified Through:
Moxifloxacin,63629-8357-2,400 mg/1,"TABLET, FILM COATED",ORAL,ANDA076938,Bryant Ranch Prepack,63629-8357,Moxifloxacin,MOXIFLOXACIN HYDROCHLORIDE,HUMAN PRESCRIPTION DRUG,11/05/2020,N/A,ANDA,"10 TABLET, FILM COATED in 1 BOTTLE (63629-8357-2)","Quinolone Antimicrobial [EPC],  Quinolones [CS]",N/A,No,12/31/2023
Moxifloxacin,31722-845-05,400 mg/1,"TABLET, FILM COATED",ORAL,ANDA204836,"Camber Pharmaceuticals, Inc.",31722-845,Moxifloxacin,MOXIFLOXACIN HYDROCHLORIDE,HUMAN PRESCRIPTION DRUG,03/02/2023,N/A,ANDA,"500 TABLET, FILM COATED in 1 BOTTLE (31722-845-05)","Quinolone Antimicrobial [EPC],  Quinolones [CS]",N/A,No,12/31/2024
Moxifloxacin,31722-845-30,400 mg/1,"TABLET, FILM COATED",ORAL,ANDA204836,"Camber Pharmaceuticals, Inc.",31722-845,Moxifloxacin,MOXIFLOXACIN HYDROCHLORIDE,HUMAN PRESCRIPTION DRUG,03/02/2023,N/A,ANDA,"30 TABLET, FILM COATED in 1 BOTTLE (31722-845-30)","Quinolone Antimicrobial [EPC],  Quinolones [CS]",N/A,No,12/31/2024
Moxifloxacin,0904-6406-04,400 mg/1,"TABLET, FILM COATED",ORAL,ANDA076938,Major Pharmaceuticals,0904-6406,Moxifloxacin,MOXIFLOXACIN HYDROCHLORIDE,HUMAN PRESCRIPTION DRUG,03/05/2014,N/A,ANDA,"30 BLISTER PACK in 1 CARTON (0904-6406-04)  / 1 TABLET, FILM COATED in 1 BLISTER PACK","Quinolone Antimicrobial [EPC],  Quinolones [CS]",N/A,No,12/31/2023
Moxifloxacin,50090-3147-0,400 mg/1,"TABLET, FILM COATED",ORAL,ANDA076938,A-S Medication Solutions,50090-3147,Moxifloxacin,MOXIFLOXACIN HYDROCHLORIDE,HUMAN PRESCRIPTION DRUG,04/25/2019,N/A,ANDA,"10 TABLET, FILM COATED in 1 BOTTLE (50090-3147-0)","Quinolone Antimicrobial [EPC],  Quinolones [CS]",N/A,No,12/31/2024
Moxifloxacin,50090-3147-1,400 mg/1,"TABLET, FILM COATED",ORAL,ANDA076938,A-S Medication Solutions,50090-3147,Moxifloxacin,MOXIFLOXACIN HYDROCHLORIDE,HUMAN PRESCRIPTION DRUG,10/02/2017,N/A,ANDA,"30 TABLET, FILM COATED in 1 BOTTLE (50090-3147-1)","Quinolone Antimicrobial [EPC],  Quinolones [CS]",N/A,No,12/31/2024
Moxifloxacin,55111-112-05,400 mg/1,"TABLET, FILM COATED",ORAL,ANDA076938,Dr. Reddy's Laboratories Limited,55111-112,Moxifloxacin,MOXIFLOXACIN HYDROCHLORIDE,HUMAN PRESCRIPTION DRUG,03/05/2014,N/A,ANDA,"500 TABLET, FILM COATED in 1 BOTTLE (55111-112-05)","Quinolone Antimicrobial [EPC],  Quinolones [CS]",N/A,No,12/31/2023
Moxifloxacin,55111-112-30,400 mg/1,"TABLET, FILM COATED",ORAL,ANDA076938,Dr. Reddy's Laboratories Limited,55111-112,Moxifloxacin,MOXIFLOXACIN HYDROCHLORIDE,HUMAN PRESCRIPTION DRUG,03/05/2014,N/A,ANDA,"30 TABLET, FILM COATED in 1 BOTTLE (55111-112-30)","Quinolone Antimicrobial [EPC],  Quinolones [CS]",N/A,No,12/31/2023
Moxifloxacin,70518-3713-0,400 mg/1,"TABLET, FILM COATED",ORAL,ANDA076938,REMEDYREPACK INC.,70518-3713,Moxifloxacin,MOXIFLOXACIN HYDROCHLORIDE,HUMAN PRESCRIPTION DRUG,04/12/2023,N/A,ANDA,"7 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3713-0)","Quinolone Antimicrobial [EPC],  Quinolones [CS]",N/A,No,12/31/2024
Moxifloxacin,50090-5833-0,400 mg/1,"TABLET, FILM COATED",ORAL,ANDA076938,A-S Medication Solutions,50090-5833,Moxifloxacin,MOXIFLOXACIN HYDROCHLORIDE,HUMAN PRESCRIPTION DRUG,10/27/2021,N/A,ANDA,"10 TABLET, FILM COATED in 1 BOTTLE (50090-5833-0)","Quinolone Antimicrobial [EPC],  Quinolones [CS]",N/A,No,12/31/2024
Moxifloxacin,55111-112-01,400 mg/1,"TABLET, FILM COATED",ORAL,ANDA076938,Dr. Reddy's Laboratories Limited,55111-112,Moxifloxacin,MOXIFLOXACIN HYDROCHLORIDE,HUMAN PRESCRIPTION DRUG,03/05/2014,N/A,ANDA,"100 TABLET, FILM COATED in 1 BOTTLE (55111-112-01)","Quinolone Antimicrobial [EPC],  Quinolones [CS]",N/A,No,12/31/2023
Moxifloxacin,72789-233-10,400 mg/1,"TABLET, FILM COATED",ORAL,ANDA076938,"PD-Rx Pharmaceuticals, Inc.",72789-233,Moxifloxacin,MOXIFLOXACIN HYDROCHLORIDE,HUMAN PRESCRIPTION DRUG,02/15/2022,N/A,ANDA,"10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-233-10)","Quinolone Antimicrobial [EPC],  Quinolones [CS]",N/A,No,12/31/2023
Moxifloxacin,0904-6406-06,400 mg/1,"TABLET, FILM COATED",ORAL,ANDA076938,Major Pharmaceuticals,0904-6406,Moxifloxacin,MOXIFLOXACIN HYDROCHLORIDE,HUMAN PRESCRIPTION DRUG,03/05/2014,N/A,ANDA,"50 BLISTER PACK in 1 CARTON (0904-6406-06)  / 1 TABLET, FILM COATED in 1 BLISTER PACK","Quinolone Antimicrobial [EPC],  Quinolones [CS]",N/A,No,12/31/2023
Moxifloxacin,63629-8357-1,400 mg/1,"TABLET, FILM COATED",ORAL,ANDA076938,Bryant Ranch Prepack,63629-8357,Moxifloxacin,MOXIFLOXACIN HYDROCHLORIDE,HUMAN PRESCRIPTION DRUG,09/17/2020,N/A,ANDA,"7 TABLET, FILM COATED in 1 BOTTLE (63629-8357-1)","Quinolone Antimicrobial [EPC],  Quinolones [CS]",N/A,No,12/31/2023
Moxifloxacin,55111-112-66,400 mg/1,"TABLET, FILM COATED",ORAL,ANDA076938,Dr. Reddy's Laboratories Limited,55111-112,Moxifloxacin,MOXIFLOXACIN HYDROCHLORIDE,HUMAN PRESCRIPTION DRUG,03/05/2014,N/A,ANDA,"5 BLISTER PACK in 1 CARTON (55111-112-66)  / 10 TABLET, FILM COATED in 1 BLISTER PACK (55111-112-79)","Quinolone Antimicrobial [EPC],  Quinolones [CS]",N/A,No,12/31/2023
MOXIFLOXACIN HYDROCHLORIDE,65862-603-30,400 mg/1,"TABLET, FILM COATED",ORAL,ANDA202632,Aurobindo Pharma Limited,65862-603,moxifloxacin hydrochloride,MOXIFLOXACIN HYDROCHLORIDE,HUMAN PRESCRIPTION DRUG,03/04/2014,N/A,ANDA,"30 TABLET, FILM COATED in 1 BOTTLE (65862-603-30)","Quinolone Antimicrobial [EPC],  Quinolones [CS]",N/A,No,12/31/2023
MOXIFLOXACIN HYDROCHLORIDE,65862-603-55,400 mg/1,"TABLET, FILM COATED",ORAL,ANDA202632,Aurobindo Pharma Limited,65862-603,moxifloxacin hydrochloride,MOXIFLOXACIN HYDROCHLORIDE,HUMAN PRESCRIPTION DRUG,03/04/2014,N/A,ANDA,"50 BLISTER PACK in 1 BOX, UNIT-DOSE (65862-603-55)  / 1 TABLET, FILM COATED in 1 BLISTER PACK (65862-603-10)","Quinolone Antimicrobial [EPC],  Quinolones [CS]",N/A,No,12/31/2023
Moxifloxacin Hydrochloride,60429-893-30,400 mg/1,TABLET,ORAL,ANDA205348,"Golden State Medical Supply, Inc.",60429-893,Moxifloxacin Hydrochloride,MOXIFLOXACIN HYDROCHLORIDE,HUMAN PRESCRIPTION DRUG,10/09/2017,N/A,ANDA,30 TABLET in 1 BOTTLE (60429-893-30),"Quinolone Antimicrobial [EPC],  Quinolones [CS]",N/A,No,12/31/2024
Moxifloxacin Hydrochloride,40032-034-03,400 mg/1,TABLET,ORAL,ANDA207285,"Novel Laboratories, Inc.",40032-034,Moxifloxacin Hydrochloride,MOXIFLOXACIN HYDROCHLORIDE,HUMAN PRESCRIPTION DRUG,02/13/2017,N/A,ANDA,"30 TABLET in 1 BOTTLE, PLASTIC (40032-034-03)","Quinolone Antimicrobial [EPC],  Quinolones [CS]",N/A,No,12/31/2023
Moxifloxacin Hydrochloride,51991-943-33,400 mg/1,TABLET,ORAL,ANDA205348,"Breckenridge Pharmaceutical, Inc.",51991-943,Moxifloxacin Hydrochloride,MOXIFLOXACIN HYDROCHLORIDE,HUMAN PRESCRIPTION DRUG,05/02/2017,N/A,ANDA,30 TABLET in 1 BOTTLE (51991-943-33),"Quinolone Antimicrobial [EPC],  Quinolones [CS]",N/A,No,12/31/2024
MOXIFLOXACIN HYDROCHLORIDE,65862-603-99,400 mg/1,"TABLET, FILM COATED",ORAL,ANDA202632,Aurobindo Pharma Limited,65862-603,moxifloxacin hydrochloride,MOXIFLOXACIN HYDROCHLORIDE,HUMAN PRESCRIPTION DRUG,03/04/2014,N/A,ANDA,"1000 TABLET, FILM COATED in 1 BOTTLE (65862-603-99)","Quinolone Antimicrobial [EPC],  Quinolones [CS]",N/A,No,12/31/2023
MOXIFLOXACIN HYDROCHLORIDE,72789-037-10,400 mg/1,"TABLET, FILM COATED",ORAL,ANDA202632,"PD-Rx Pharmaceuticals, Inc.",72789-037,moxifloxacin hydrochloride,MOXIFLOXACIN HYDROCHLORIDE,HUMAN PRESCRIPTION DRUG,02/17/2020,N/A,ANDA,"10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-037-10)","Quinolone Antimicrobial [EPC],  Quinolones [CS]",N/A,No,12/31/2023
MOXIFLOXACIN HYDROCHLORIDE,72789-038-10,400 mg/1,"TABLET, FILM COATED",ORAL,ANDA202632,"PD-Rx Pharmaceuticals, Inc.",72789-038,moxifloxacin hydrochloride,MOXIFLOXACIN HYDROCHLORIDE,HUMAN PRESCRIPTION DRUG,12/10/2019,N/A,ANDA,"10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-038-10)","Quinolone Antimicrobial [EPC],  Quinolones [CS]",N/A,No,12/31/2023
Moxifloxacin Hydrochloride,50090-4058-1,400 mg/1,TABLET,ORAL,ANDA205348,A-S Medication Solutions,50090-4058,Moxifloxacin Hydrochloride,MOXIFLOXACIN HYDROCHLORIDE,HUMAN PRESCRIPTION DRUG,01/15/2019,N/A,ANDA,30 TABLET in 1 BOTTLE (50090-4058-1),"Quinolone Antimicrobial [EPC],  Quinolones [CS]",N/A,No,12/31/2024
Moxifloxacin Hydrochloride,50090-4100-0,400 mg/1,TABLET,ORAL,ANDA205348,A-S Medication Solutions,50090-4100,Moxifloxacin Hydrochloride,MOXIFLOXACIN HYDROCHLORIDE,HUMAN PRESCRIPTION DRUG,01/25/2019,N/A,ANDA,10 TABLET in 1 BOTTLE (50090-4100-0),"Quinolone Antimicrobial [EPC],  Quinolones [CS]",N/A,No,12/31/2024
Moxifloxacin Hydrochloride,57237-156-30,400 mg/1,"TABLET, FILM COATED",ORAL,ANDA202632,"Rising Health, LLC",57237-156,Moxifloxacin Hydrochloride,MOXIFLOXACIN HYDROCHLORIDE,HUMAN PRESCRIPTION DRUG,03/04/2014,N/A,ANDA,"30 TABLET, FILM COATED in 1 BOTTLE (57237-156-30)","Quinolone Antimicrobial [EPC],  Quinolones [CS]",N/A,No,12/31/2023
Moxifloxacin Hydrochloride,40032-034-05,400 mg/1,TABLET,ORAL,ANDA207285,"Novel Laboratories, Inc.",40032-034,Moxifloxacin Hydrochloride,MOXIFLOXACIN HYDROCHLORIDE,HUMAN PRESCRIPTION DRUG,02/13/2017,N/A,ANDA,"500 TABLET in 1 BOTTLE, PLASTIC (40032-034-05)","Quinolone Antimicrobial [EPC],  Quinolones [CS]",N/A,No,12/31/2023
Moxifloxacin Hydrochloride,68084-722-65,400 mg/1,"TABLET, FILM COATED",ORAL,ANDA202632,American Health Packaging,68084-722,Moxifloxacin Hydrochloride,MOXIFLOXACIN HYDROCHLORIDE,HUMAN PRESCRIPTION DRUG,03/19/2014,N/A,ANDA,"50 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-722-65)  / 1 TABLET, FILM COATED in 1 BLISTER PACK (68084-722-11)","Quinolone Antimicrobial [EPC],  Quinolones [CS]",N/A,No,12/31/2023
moxifloxacin hydrochloride,13668-201-01,400 mg/1,TABLET,ORAL,ANDA200160,Torrent Pharmaceuticals Limited,13668-201,moxifloxacin hydrochloride,MOXIFLOXACIN HYDROCHLORIDE,HUMAN PRESCRIPTION DRUG,04/03/2014,05/31/2024,ANDA,100 TABLET in 1 BOTTLE (13668-201-01),"Quinolone Antimicrobial [EPC],  Quinolones [CS]",N/A,No,N/A
moxifloxacin hydrochloride,13668-201-05,400 mg/1,TABLET,ORAL,ANDA200160,Torrent Pharmaceuticals Limited,13668-201,moxifloxacin hydrochloride,MOXIFLOXACIN HYDROCHLORIDE,HUMAN PRESCRIPTION DRUG,04/03/2014,05/31/2024,ANDA,500 TABLET in 1 BOTTLE (13668-201-05),"Quinolone Antimicrobial [EPC],  Quinolones [CS]",N/A,No,N/A
moxifloxacin hydrochloride,13668-201-30,400 mg/1,TABLET,ORAL,ANDA200160,Torrent Pharmaceuticals Limited,13668-201,moxifloxacin hydrochloride,MOXIFLOXACIN HYDROCHLORIDE,HUMAN PRESCRIPTION DRUG,04/03/2014,05/31/2024,ANDA,30 TABLET in 1 BOTTLE (13668-201-30),"Quinolone Antimicrobial [EPC],  Quinolones [CS]",N/A,No,N/A
Moxifloxacin Hydrochloride,40032-034-31,400 mg/1,TABLET,ORAL,ANDA207285,"Novel Laboratories, Inc.",40032-034,Moxifloxacin Hydrochloride,MOXIFLOXACIN HYDROCHLORIDE,HUMAN PRESCRIPTION DRUG,02/13/2017,N/A,ANDA,5 BLISTER PACK in 1 CARTON (40032-034-31)  / 10 TABLET in 1 BLISTER PACK,"Quinolone Antimicrobial [EPC],  Quinolones [CS]",N/A,No,12/31/2023
Moxifloxacin Hydrochloride,0093-7387-56,400 mg/1,"TABLET, FILM COATED",ORAL,ANDA077437,"Teva Pharmaceuticals USA, Inc.",0093-7387,Moxifloxacin Hydrochloride,MOXIFLOXACIN HYDROCHLORIDE,HUMAN PRESCRIPTION DRUG,02/19/2014,N/A,ANDA,"30 TABLET, FILM COATED in 1 BOTTLE (0093-7387-56)","Quinolone Antimicrobial [EPC],  Quinolones [CS]",N/A,No,12/31/2023
Moxifloxacin Hydrochloride,67296-1616-5,400 mg/1,"TABLET, FILM COATED",ORAL,ANDA202632,"RedPharm Drug, Inc.",67296-1616,Moxifloxacin Hydrochloride,MOXIFLOXACIN HYDROCHLORIDE,HUMAN PRESCRIPTION DRUG,01/01/2018,N/A,ANDA,"5 TABLET, FILM COATED in 1 BOTTLE (67296-1616-5)","Quinolone Antimicrobial [EPC],  Quinolones [CS]",N/A,No,12/31/2023
Moxifloxacin Hydrochloride,50268-576-13,400 mg/1,"TABLET, FILM COATED",ORAL,ANDA202632,AvPAK,50268-576,Moxifloxacin Hydrochloride,MOXIFLOXACIN HYDROCHLORIDE,HUMAN PRESCRIPTION DRUG,07/22/2016,N/A,ANDA,"30 BLISTER PACK in 1 BOX, UNIT-DOSE (50268-576-13)  / 1 TABLET, FILM COATED in 1 BLISTER PACK (50268-576-11)","Quinolone Antimicrobial [EPC],  Quinolones [CS]",N/A,No,12/31/2023
"Moxifloxacin Hydrochloride Tablets, 400 mg",72205-001-05,400 mg/1,"TABLET, FILM COATED",ORAL,ANDA208682,Novadoz Pharmaceuticals LLC,72205-001,"Moxifloxacin Hydrochloride Tablets, 400 mg",MOXIFLOXACIN HYDROCHLORIDE MONOHYDRATE,HUMAN PRESCRIPTION DRUG,04/16/2019,N/A,ANDA,"500 TABLET, FILM COATED in 1 BOTTLE (72205-001-05)","Quinolone Antimicrobial [EPC],  Quinolones [CS]",N/A,No,12/31/2023
"Moxifloxacin Hydrochloride Tablets, 400 mg",72205-001-30,400 mg/1,"TABLET, FILM COATED",ORAL,ANDA208682,Novadoz Pharmaceuticals LLC,72205-001,"Moxifloxacin Hydrochloride Tablets, 400 mg",MOXIFLOXACIN HYDROCHLORIDE MONOHYDRATE,HUMAN PRESCRIPTION DRUG,04/16/2019,N/A,ANDA,"30 TABLET, FILM COATED in 1 BOTTLE (72205-001-30)","Quinolone Antimicrobial [EPC],  Quinolones [CS]",N/A,No,12/31/2023
"Moxifloxacin Hydrochloride Tablets, 400 mg",72205-001-31,400 mg/1,"TABLET, FILM COATED",ORAL,ANDA208682,Novadoz Pharmaceuticals LLC,72205-001,"Moxifloxacin Hydrochloride Tablets, 400 mg",MOXIFLOXACIN HYDROCHLORIDE MONOHYDRATE,HUMAN PRESCRIPTION DRUG,04/16/2019,N/A,ANDA,"50 BLISTER PACK in 1 CARTON (72205-001-31)  / 10 TABLET, FILM COATED in 1 BLISTER PACK (72205-001-11)","Quinolone Antimicrobial [EPC],  Quinolones [CS]",N/A,No,12/31/2023
"Moxifloxacin Hydrochloride Tablets, 400 mg",72789-080-10,400 mg/1,"TABLET, FILM COATED",ORAL,ANDA208682,"PD-Rx Pharmaceuticals, Inc.",72789-080,"Moxifloxacin Hydrochloride Tablets, 400 mg",MOXIFLOXACIN HYDROCHLORIDE MONOHYDRATE,HUMAN PRESCRIPTION DRUG,04/10/2020,N/A,ANDA,"10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-080-10)","Quinolone Antimicrobial [EPC],  Quinolones [CS]",N/A,No,12/31/2023
"Moxifloxacin Hydrochloride Tablets, 400 mg",69539-006-30,400 mg/1,"TABLET, FILM COATED",ORAL,ANDA208682,MSN LABORATORIES PRIVATE LIMITED,69539-006,"Moxifloxacin Hydrochloride Tablets, 400 mg",MOXIFLOXACIN HYDROCHLORIDE MONOHYDRATE,HUMAN PRESCRIPTION DRUG,04/16/2019,N/A,ANDA,"30 TABLET, FILM COATED in 1 BOTTLE (69539-006-30)","Quinolone Antimicrobial [EPC],  Quinolones [CS]",N/A,No,12/31/2023
"Moxifloxacin Hydrochloride Tablets, 400 mg",69539-006-31,400 mg/1,"TABLET, FILM COATED",ORAL,ANDA208682,MSN LABORATORIES PRIVATE LIMITED,69539-006,"Moxifloxacin Hydrochloride Tablets, 400 mg",MOXIFLOXACIN HYDROCHLORIDE MONOHYDRATE,HUMAN PRESCRIPTION DRUG,04/16/2019,N/A,ANDA,"50 BLISTER PACK in 1 CARTON (69539-006-31)  / 10 TABLET, FILM COATED in 1 BLISTER PACK (69539-006-11)","Quinolone Antimicrobial [EPC],  Quinolones [CS]",N/A,No,12/31/2023
"Moxifloxacin Hydrochloride Tablets, 400 mg",69539-006-05,400 mg/1,"TABLET, FILM COATED",ORAL,ANDA208682,MSN LABORATORIES PRIVATE LIMITED,69539-006,"Moxifloxacin Hydrochloride Tablets, 400 mg",MOXIFLOXACIN HYDROCHLORIDE MONOHYDRATE,HUMAN PRESCRIPTION DRUG,04/16/2019,N/A,ANDA,"500 TABLET, FILM COATED in 1 BOTTLE (69539-006-05)","Quinolone Antimicrobial [EPC],  Quinolones [CS]",N/A,No,12/31/2023