FDA NDC Directory · JSON-LD · Markdown

Acetaminophen

NDC 79481-0184 · HUMAN OTC DRUG · TABLET

Labeler / ManufacturerMEIJER, INC.
Marketing categoryAbbreviated NDA (generic) · App ANDA211544
Dosage form / routeTABLET · ORAL
Active ingredientsACETAMINOPHEN (650 mg/1)
Marketing started20230717
Package count2

External sources

Source: openFDA. Public-domain (CC0).