Metronidazole

Product NDC
50090-5687
11-digit product format
500905687
Labeler code
50090
Product ID
50090-5687_66b1da4c-2833-49ef-9f42-151dd8d99fcd
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Metronidazole
Dosage form
TABLET
Route
ORAL
Labeler
A-S Medication Solutions
Application
ANDA203974
Marketing category
ANDA
Marketing start
2015-05-29
Marketing end
0000-00-00
Substance
METRONIDAZOLE
Active strength
500 mg/1
Pharmacologic classes
Nitroimidazole Antimicrobial [EPC],Nitroimidazoles [CS]
NDC exclude flag
No
Listing certified through
2022-12-31
Current FDA listing
Historical FDA.report record

Related Records

Related UNII Ingredients

UNIIPreferred termRegistry numberMatched term
140QMO216EMETRONIDAZOLE443-48-1METRONIDAZOLE

Packages

Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
50090-5687-0500905687004 TABLET in 1 BOTTLE (50090-5687-0) 4 tablet2021-09-210000-00-00NoNoCurrent
50090-5687-35009056870314 TABLET in 1 BOTTLE (50090-5687-3) 14 tablet2021-09-210000-00-00NoNoCurrent
50090-5687-45009056870421 TABLET in 1 BOTTLE (50090-5687-4) 21 tablet2021-09-210000-00-00NoNoCurrent
50090-5687-65009056870628 TABLET in 1 BOTTLE (50090-5687-6) 28 tablet2021-09-210000-00-00NoNoCurrent
50090-5687-95009056870920 TABLET in 1 BOTTLE (50090-5687-9) 20 tablet2021-09-210000-00-00NoNoCurrent