FDA NDC Directory · JSON-LD · Markdown

8 hr Arthritis Pain Relief

NDC 55910-892 · HUMAN OTC DRUG · TABLET, EXTENDED RELEASE

Generic nameAcetaminophen
Labeler / ManufacturerDOLGENCORP, INC.
Marketing categoryAbbreviated NDA (generic) · App ANDA215486
Dosage form / routeTABLET, EXTENDED RELEASE · ORAL
Active ingredientsACETAMINOPHEN (650 mg/1)
Marketing started20230429
Package count3

External sources

Source: openFDA. Public-domain (CC0).