Naproxen

Product NDC
72189-425
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Naproxen
Dosage form
TABLET
Route
ORAL
Labeler
Direct_Rx
Application
ANDA212517
Marketing category
ANDA
Substance
NAPROXEN
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
72189-425-3030 TABLET in 1 BOTTLE (72189-425-30) 2023-02-13NoHistorical
72189-425-6060 TABLET in 1 BOTTLE (72189-425-60) 2023-02-13NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
NaproxenDirect_Rx2025-01-22HUMAN PRESCRIPTION DRUG LABEL3