Lorazepam

Product NDC
68071-5022
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Lorazepam
Dosage form
TABLET
Route
ORAL
Labeler
NuCare Pharmaceuticals,Inc.
Application
ANDA203572
Marketing category
ANDA
Substance
LORAZEPAM
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
68071-5022-515 TABLET in 1 BOTTLE (68071-5022-5) 2019-08-08NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Lorazepam Tablets USP CIVNuCare Pharmaceuticals,Inc.2024-10-09HUMAN PRESCRIPTION DRUG LABEL5