Metronidazole

Product NDC
63629-7754
11-digit product format
636297754
Labeler code
63629
Product ID
63629-7754_47b35461-d4ef-467c-9ea7-46310e3e1439
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Metronidazole
Dosage form
TABLET
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA070027
Marketing category
ANDA
Marketing start
1990-09-30
Marketing end
0000-00-00
Substance
METRONIDAZOLE
Active strength
250 mg/1
Pharmacologic classes
Nitroimidazole Antimicrobial [EPC],Nitroimidazoles [CS]
NDC exclude flag
No
Listing certified through
2021-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
63629-7754-16362977540128 TABLET in 1 BOTTLE (63629-7754-1) 28 tablet2005-11-090000-00-00NoNoCurrent
63629-7754-2636297754028 TABLET in 1 BOTTLE (63629-7754-2) 8 tablet2005-11-090000-00-00NoNoCurrent
63629-7754-36362977540314 TABLET in 1 BOTTLE (63629-7754-3) 14 tablet2005-11-090000-00-00NoNoCurrent
63629-7754-46362977540421 TABLET in 1 BOTTLE (63629-7754-4) 21 tablet2005-11-090000-00-00NoNoCurrent
63629-7754-56362977540530 TABLET in 1 BOTTLE (63629-7754-5) 30 tablet2005-11-090000-00-00NoNoCurrent
63629-7754-663629775406300 TABLET in 1 BOTTLE (63629-7754-6) 300 tablet2005-11-090000-00-00NoNoCurrent