NDC 65862-309 – Fosinopril Sodium and Hydrochlorothiazide
Fosinopril Sodium 20 mg/1; Hydrochlorothiazide 12.5 mg/1 · Tablet · Oral
Product NDC65862-309
Product details
- Brand name
- Fosinopril Sodium and Hydrochlorothiazide
- Generic name
- Fosinopril Sodium and Hydrochlorothiazide
- Labeler
- Aurobindo Pharma Limited
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA079245
- Marketed since
- July 9, 2009
- Listing expires
- December 31, 2026
- Pharmacologic class
- Angiotensin Converting Enzyme Inhibitor; Thiazide Diuretic
Active ingredients
- Fosinopril Sodium 20 mg/1
- Hydrochlorothiazide 12.5 mg/1
Uses, dosage, side effects and warnings for Fosinopril Sodium and Hydrochlorothiazide →
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 65862-309-01 | 100 TABLET in 1 BOTTLE (65862-309-01) | Jul 9, 2009 |
| 65862-309-30 | 30 TABLET in 1 BOTTLE (65862-309-30) | Jul 9, 2009 |
| 65862-309-99 | 1000 TABLET in 1 BOTTLE (65862-309-99) | Jul 9, 2009 |