FDA NDC Directory · JSON-LD · Markdown

Acetaminophen

NDC 63868-660 · HUMAN OTC DRUG · TABLET, EXTENDED RELEASE

Labeler / ManufacturerCHAIN DRUG MARKETING ASSOCIATION INC
Marketing categoryAbbreviated NDA (generic) · App ANDA211544
Dosage form / routeTABLET, EXTENDED RELEASE · ORAL
Active ingredientsACETAMINOPHEN (650 mg/1)
Marketing started20200801
Marketing ended20261231
Package count2

External sources

Source: openFDA. Public-domain (CC0).