FDA NDC Directory · JSON-LD · Markdown

Ibuprofen

NDC 49483-114 · HUMAN OTC DRUG · TABLET, FILM COATED

Labeler / ManufacturerTIME CAP LABORATORIES,INC
Marketing categoryAbbreviated NDA (generic) · App ANDA091239
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsIBUPROFEN (200 mg/1)
Marketing started20160322
Package count4

External sources

Source: openFDA. Public-domain (CC0).