Clonazepam

Product NDC
70518-3849
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Clonazepam
Dosage form
TABLET
Route
ORAL
Labeler
REMEDYREPACK INC.
Application
ANDA075150
Marketing category
ANDA
Substance
CLONAZEPAM
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
70518-3849-230 TABLET in 1 BLISTER PACK (70518-3849-2) 2024-02-21NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Clonazepam Tablets, USP CIV 0.5 mg, 1 mg and 2 mg Rx onlyREMEDYREPACK INC.2025-04-24HUMAN PRESCRIPTION DRUG LABEL3