FDA NDC Directory · JSON-LD · Markdown

Acetaminophen, Ibuprofen

NDC 72657-157 · HUMAN OTC DRUG · TABLET, FILM COATED

Labeler / ManufacturerGLENMARK THERAPEUTICS INC., USA
Marketing categoryAbbreviated NDA (generic) · App ANDA218311
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsACETAMINOPHEN (250 mg/1)
IBUPROFEN (125 mg/1)
Marketing started20240507
Package count7

External sources

Source: openFDA. Public-domain (CC0).