NDC 0078-1518 – Amlodipine valsartan and hydrochlorothiazide
Amlodipine Besylate 10 mg/1; Valsartan 160 mg/1; Hydrochlorothiazide 12.5 mg/1 · Tablet, Film Coated
Product NDC0078-1518
Product details
- Brand name
- Amlodipine valsartan and hydrochlorothiazide
- Generic name
- Amlodipine valsartan and hydrochlorothiazide
- Labeler
- Novartis Pharmaceuticals Corporation
- Dosage form
- Tablet, Film Coated
- Marketing category
- DRUG FOR FURTHER PROCESSING
- Marketed since
- April 4, 2009
- Listing expires
- December 31, 2027
Active ingredients
- Amlodipine Besylate 10 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 (1)
| Package NDC | Description | Since |
|---|---|---|
| 0078-1518-01 | 60000 TABLET, FILM COATED in 1 DRUM (0078-1518-01) |
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