FDA NDC Directory · JSON-LD · Markdown

Katerzia

NDC 52652-5001 · HUMAN PRESCRIPTION DRUG · SUSPENSION

Generic nameAmlodipine
Labeler / ManufacturerAzurity Pharmaceuticals, Inc.
Marketing categoryNew Drug Application (innovator) · App NDA211340
Dosage form / routeSUSPENSION · ORAL
Active ingredientsAMLODIPINE BENZOATE (1 mg/mL)
Marketing started20190815
Package count1

External sources

Source: openFDA. Public-domain (CC0).