NDC 0093-5150 – Moexipril Hydrochloride
Moexipril Hydrochloride 15 mg/1 · Tablet, Film Coated · Oral
Product NDC0093-5150
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 15 mg/1
Uses, dosage, side effects and warnings for Moexipril Hydrochloride →
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 0093-5150-01 | 100 TABLET, FILM COATED in 1 BOTTLE (0093-5150-01) | May 8, 2003 |
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