FDA NDC Directory · JSON-LD · Markdown

Acetaminophen

NDC 68001-495 · HUMAN OTC DRUG · TABLET

Labeler / ManufacturerBluePoint Laboratories
Marketing categoryAbbreviated NDA (generic) · App ANDA207229
Dosage form / routeTABLET · ORAL
Active ingredientsACETAMINOPHEN (650 mg/1)
Marketing started20210430
Package count1

External sources

Source: openFDA. Public-domain (CC0).