metronidazole

Product NDC
68382-850
11-digit product format
683820850
Labeler code
68382
Product ID
68382-850_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
250 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
68382-850-01EA - Each68382-850a4f05144-1e1f-4149-898c-1ce3f048794a12018-05-09
68382-850-05EA - Each68382-85028c1a7f4-a6d8-456b-9663-0571d1eb645d12018-04-19
68382-850-21EA - Each68382-8503d21db79-7f7c-4f19-8375-01ea9e74e2ff12018-05-09