NDC 0093-0017 – Moexipril Hydrochloride
Moexipril Hydrochloride 7.5 mg/1 · Tablet, Film Coated · Oral
Product NDC0093-0017
Product details
- Brand name
- Moexipril Hydrochloride
- Generic name
- Moexipril Hydrochloride
- Labeler
- Teva Pharmaceuticals USA, Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA076204
- Marketed since
- May 8, 2003
- Listing expires
- December 31, 2026
- Pharmacologic class
- Angiotensin Converting Enzyme Inhibitor
Active ingredients
- Moexipril Hydrochloride 7.5 mg/1
Uses, dosage, side effects and warnings for Moexipril Hydrochloride →
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 0093-0017-01 | 100 TABLET, FILM COATED in 1 BOTTLE (0093-0017-01) | May 8, 2003 |
Other Moexipril Hydrochloride products
- 62135-967 Moexipril Hydrochloride 7.5 mg/1 · Tablet, Film Coated · Chartwell RX, LLC
- 62135-969 Moexipril Hydrochloride 15 mg/1 · Tablet, Film Coated · Chartwell RX, LLC
- 68462-208 Moexipril Hydrochloride 15 mg/1 · Tablet, Film Coated · Glenmark Pharmaceuticals Inc., USA
- 68462-209 Moexipril Hydrochloride 7.5 mg/1 · Tablet, Film Coated · Glenmark Pharmaceuticals Inc., USA
- 0093-5150 Moexipril Hydrochloride 15 mg/1 · Tablet, Film Coated · Teva Pharmaceuticals USA, Inc.