FDA NDC Directory · JSON-LD · Markdown

Ibuprofen

NDC 68016-813 · HUMAN OTC DRUG · CAPSULE, LIQUID FILLED

Labeler / ManufacturerChain Drug Consortium, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA206568
Dosage form / routeCAPSULE, LIQUID FILLED · ORAL
Active ingredientsIBUPROFEN (200 mg/1)
Marketing started20220826
Marketing ended20261231
Package count1

External sources

Source: openFDA. Public-domain (CC0).