Naproxen

Product NDC
70518-4514
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Naproxen
Dosage form
TABLET
Route
ORAL
Labeler
REMEDYREPACK INC.
Application
ANDA074140
Marketing category
ANDA
Substance
NAPROXEN
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
70518-4514-030 TABLET in 1 BLISTER PACK (70518-4514-0) 2025-11-03NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
NaproxenREMEDYREPACK INC.2025-11-03HUMAN PRESCRIPTION DRUG LABEL1