# Amlodipine Besylate

NDC: 51407-950
Generic name: Amlodipine Besylate
Labeler / Manufacturer: GSMS, Incorporated
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20070523

FDA application: ANDA076719

## Active ingredients

- AMLODIPINE BESYLATE: 5 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"51407-950"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=51407-950
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=9c0f83f4-06ad-4bb1-a8e3-dcac43b840cf