FDA NDC Directory · JSON-LD · Markdown

PAROXETINE HYDROCHLORIDE

NDC 31722-578 · HUMAN PRESCRIPTION DRUG · SUSPENSION

Labeler / ManufacturerCamber Pharmaceuticals, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA219954
Dosage form / routeSUSPENSION · ORAL
Active ingredientsPAROXETINE HYDROCHLORIDE (10 mg/5mL)
Marketing started20260305
Package count1

External sources

Source: openFDA. Public-domain (CC0).