metronidazole

Product NDC
71335-1703
11-digit product format
713351703
Labeler code
71335
Product ID
71335-1703_408356ad-8fc4-409b-aa3c-83e5aacc4ece
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
metronidazole
Dosage form
TABLET
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA206560
Marketing category
ANDA
Marketing start
2019-02-23
Substance
METRONIDAZOLE
Active strength
500 mg/1
Pharmacologic classes
Nitroimidazole Antimicrobial [EPC], Nitroimidazoles [CS]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Related Records

Related UNII Ingredients

UNIIPreferred termRegistry numberMatched term
140QMO216EMETRONIDAZOLE443-48-1METRONIDAZOLE

Packages

Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
71335-1703-07133517030040 TABLET in 1 BOTTLE (71335-1703-0) 40 tablet2022-11-22NoNoHistorical
71335-1703-17133517030120 TABLET in 1 BOTTLE (71335-1703-1) 20 tablet2020-09-23NoNoHistorical
71335-1703-27133517030230 TABLET in 1 BOTTLE (71335-1703-2) 30 tablet2020-10-20NoNoHistorical
71335-1703-37133517030314 TABLET in 1 BOTTLE (71335-1703-3) 14 tablet2020-10-05NoNoHistorical
71335-1703-47133517030456 TABLET in 1 BOTTLE (71335-1703-4) 56 tablet2024-08-12NoNoHistorical
71335-1703-57133517030521 TABLET in 1 BOTTLE (71335-1703-5) 21 tablet2020-10-16NoNoHistorical
71335-1703-6713351703064 TABLET in 1 BOTTLE (71335-1703-6) 4 tablet2021-11-05NoNoHistorical
71335-1703-77133517030728 TABLET in 1 BOTTLE (71335-1703-7) 28 tablet2020-09-24NoNoHistorical
71335-1703-871335170308100 TABLET in 1 BOTTLE (71335-1703-8) 100 tablet2024-08-12NoNoHistorical
71335-1703-97133517030960 TABLET in 1 BOTTLE (71335-1703-9) 60 tablet2024-04-15NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Metronidazole Tablets, USP Rx onlyBryant Ranch Prepack2024-08-12HUMAN PRESCRIPTION DRUG LABEL105