# Amlodipine Besylate

NDC: 67877-199
Generic name: Amlodipine besylate
Labeler / Manufacturer: Ascend Laboratories, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20101020

FDA application: ANDA078925

## Active ingredients

- AMLODIPINE BESYLATE: 10 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"67877-199"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=67877-199
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=3f4703c0-0b9e-41a0-8b70-da26683d9ed2