NDC 51672-4046 – Enalapril Maleate and Hydrochlorothiazide
Enalapril Maleate 10 mg/1; Hydrochlorothiazide 25 mg/1 · Tablet · Oral
Product NDC51672-4046
Product details
- Brand name
- Enalapril Maleate and Hydrochlorothiazide
- Generic name
- Enalapril Maleate and Hydrochlorothiazide
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA075788
- Marketed since
- September 18, 2001
- Listing expires
- December 31, 2027
- Pharmacologic class
- Angiotensin Converting Enzyme Inhibitor; Thiazide Diuretic
Active ingredients
- Enalapril Maleate 10 mg/1
- Hydrochlorothiazide 25 mg/1
Uses, dosage, side effects and warnings for Enalapril maleate and hydrochlorothiazide →
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 51672-4046-1 | 100 TABLET in 1 BOTTLE (51672-4046-1) | Sep 18, 2001 |
| 51672-4046-3 | 1000 TABLET in 1 BOTTLE (51672-4046-3) | Sep 18, 2001 |
Other Enalapril maleate and hydrochlorothiazide products
- 55111-133 Enalapril Maleate 5 mg/1; Hydrochlorothiazide 12.5 mg/1 · Tablet · Dr. Reddy's Laboratories Limited
- 55111-134 Enalapril Maleate 10 mg/1; Hydrochlorothiazide 25 mg/1 · Tablet · Dr. Reddy's Laboratories Limited
- 51672-4045 Enalapril Maleate 5 mg/1; Hydrochlorothiazide 12.5 mg/1 · Tablet · Sun Pharmaceutical Industries, Inc.