NDC 62135-967 – Moexipril Hydrochloride
Moexipril Hydrochloride 7.5 mg/1 · Tablet, Film Coated · Oral
Product NDC62135-967
Product details
- Brand name
- Moexipril Hydrochloride
- Generic name
- Moexipril Hydrochloride
- Labeler
- Chartwell RX, LLC
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA077536
- Marketed since
- November 30, 2006
- 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 |
|---|---|---|
| 62135-967-90 | 90 TABLET, FILM COATED in 1 BOTTLE (62135-967-90) | Mar 5, 2025 |
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