FDA NDC Directory · JSON-LD · Markdown

IBUPROFEN

NDC 68210-0200 · HUMAN OTC DRUG · CAPSULE, LIQUID FILLED

Labeler / ManufacturerSPIRIT PHARMACEUTICALS,LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA079205
Dosage form / routeCAPSULE, LIQUID FILLED · ORAL
Active ingredientsIBUPROFEN (200 mg/1)
Marketing started20180410
Package count1

External sources

Source: openFDA. Public-domain (CC0).