NDC 68462-208 – Moexipril Hydrochloride
Moexipril Hydrochloride 15 mg/1 · Tablet, Film Coated · Oral
Product NDC68462-208
Product details
- Brand name
- Moexipril Hydrochloride
- Generic name
- Moexipril Hydrochloride
- Labeler
- Glenmark Pharmaceuticals Inc., USA
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA090416
- Marketed since
- December 31, 2010
- Listing expires
- December 31, 2027
- 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 (3)
| Package NDC | Description | Since |
|---|---|---|
| 68462-208-01 | 100 TABLET, FILM COATED in 1 BOTTLE (68462-208-01) | Dec 31, 2010 |
| 68462-208-10 | 1000 TABLET, FILM COATED in 1 BOTTLE (68462-208-10) | Dec 31, 2010 |
| 68462-208-90 | 90 TABLET, FILM COATED in 1 BOTTLE (68462-208-90) | Dec 31, 2010 |
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