metronidazole

Product NDC
68382-851
11-digit product format
683820851
Labeler code
68382
Product ID
68382-851_4d54fa70-356a-4111-b909-61475e772c03
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
metronidazole
Dosage form
TABLET
Route
ORAL
Labeler
Zydus Pharmaceuticals (USA) Inc.
Application
ANDA206560
Marketing category
ANDA
Marketing start
2017-01-19
Marketing end
2019-11-30
Substance
METRONIDAZOLE
Active strength
500 mg/1
Pharmacologic classes
Nitroimidazole Antimicrobial [EPC],Nitroimidazoles [CS]
NDC exclude flag
No
Listing certified through
0000-00-00
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
68382-851-01EA - Each68382-851d5f5a8ab-1f2a-4b62-85d0-afb0eda4aa4112018-04-19
68382-851-05EA - Each68382-8511b01fa5e-5974-477f-8305-cd5c3a5d858d12018-05-09
68382-851-18EA - Each68382-8511cbc3aae-f4ae-49d9-b1d4-96a594bd73b312018-05-09