NDC 65862-834 – Amlodipine, Valsartan and Hydrochlorothiazide
Amlodipine Besylate 5 mg/1; Valsartan 160 mg/1; Hydrochlorothiazide 12.5 mg/1 · Tablet, Film Coated · Oral
Product NDC65862-834
Product details
- Brand name
- Amlodipine, Valsartan and Hydrochlorothiazide
- Generic name
- Amlodipine, Valsartan and Hydrochlorothiazide
- Labeler
- Aurobindo Pharma Limited
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA206180
- Marketed since
- December 19, 2017
- Listing expires
- December 31, 2026
- Pharmacologic class
- Angiotensin 2 Receptor Blocker; Calcium Channel Blocker; Dihydropyridine Calcium Channel Blocker; Thiazide Diuretic
Active ingredients
- Amlodipine Besylate 5 mg/1
- Valsartan 160 mg/1
- Hydrochlorothiazide 12.5 mg/1
Uses, dosage, side effects and warnings for Amlodipine,valsartan and hydrochlorothiazide →
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 65862-834-05 | 500 TABLET, FILM COATED in 1 BOTTLE (65862-834-05) | Dec 19, 2017 |
| 65862-834-30 | 30 TABLET, FILM COATED in 1 BOTTLE (65862-834-30) | Dec 19, 2017 |
| 65862-834-90 | 90 TABLET, FILM COATED in 1 BOTTLE (65862-834-90) | Dec 19, 2017 |
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