# amlodipine and valsartan

NDC: 33342-282
Generic name: amlodipine and valsartan
Labeler / Manufacturer: Macleods Pharmaceuticals Limited
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20241016

FDA application: ANDA207292

## Active ingredients

- AMLODIPINE BESYLATE: 10 mg/1
- VALSARTAN: 320 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"33342-282"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=33342-282
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=5dfadaf0-c333-4b79-9a97-e42f77505c40