NDC 69097-857 – Fosinopril Sodium
Fosinopril Sodium 20 mg/1 · Tablet · Oral
Product NDC69097-857
Product details
- Brand name
- Fosinopril Sodium
- Generic name
- Fosinopril
- Labeler
- Cipla USA Inc.
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA077222
- Marketed since
- June 16, 2016
- Listing expires
- December 31, 2026
- Pharmacologic class
- Angiotensin Converting Enzyme Inhibitor
Active ingredients
- Fosinopril Sodium 20 mg/1
Uses, dosage, side effects and warnings for Fosinopril Sodium →
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 69097-857-05 | 90 TABLET in 1 BOTTLE (69097-857-05) | Jun 16, 2016 |
| 69097-857-15 | 1000 TABLET in 1 BOTTLE (69097-857-15) | Jun 16, 2016 |
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