FDA NDC Directory · JSON-LD · Markdown

HEB

NDC 37808-120 · HUMAN OTC DRUG · TABLET, EXTENDED RELEASE

Generic nameAcetaminophen
Labeler / ManufacturerHEB
Marketing categoryAbbreviated NDA (generic) · App ANDA211544
Dosage form / routeTABLET, EXTENDED RELEASE · ORAL
Active ingredientsACETAMINOPHEN (650 mg/1)
Marketing started20200301
Package count2

External sources

Source: openFDA. Public-domain (CC0).