# Amlodipine Besylate

NDC: 29300-396
Generic name: Amlodipine Besylate
Labeler / Manufacturer: Unichem Pharmaceuticals (USA), Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20190522

FDA application: ANDA203245

## Active ingredients

- AMLODIPINE BESYLATE: 2.5 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"29300-396"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=29300-396
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=a516b336-8f60-4b86-8921-c7d6c07629f2