FDA NDC Directory · JSON-LD · Markdown

Ranitidine

NDC 0121-0727 · HUMAN PRESCRIPTION DRUG · SYRUP

Generic nameRANITIDINE
Labeler / ManufacturerPharmaceutical Associates, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA077405
Dosage form / routeSYRUP · ORAL
Active ingredientsRANITIDINE (15 mg/mL)
Marketing started20101101
Package count1

External sources

Source: openFDA. Public-domain (CC0).