FDA NDC Directory · JSON-LD · Markdown

Dual Action Pain Relief

NDC 49483-716 · HUMAN OTC DRUG · TABLET

Generic nameAcetaminophen, Ibuprofen
Labeler / ManufacturerTIME CAP LABORATORIES, INC.
Marketing categoryAbbreviated NDA (generic) · App ANDA216994
Dosage form / routeTABLET · ORAL
Active ingredientsACETAMINOPHEN (250 mg/1)
IBUPROFEN (125 mg/1)
Marketing started20231013
Package count2

External sources

Source: openFDA. Public-domain (CC0).