NDC 71335-0381 – Fosinopril Sodium
Fosinopril Sodium 10 mg/1 · Tablet · Oral
Product NDC71335-0381
Product details
- Brand name
- Fosinopril Sodium
- Generic name
- Fosinopril
- Labeler
- Bryant Ranch Prepack
- 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 10 mg/1
Uses, dosage, side effects and warnings for Fosinopril Sodium →
Package NDC codes (4)
| Package NDC | Description | Since |
|---|---|---|
| 71335-0381-1 | 30 TABLET in 1 BOTTLE (71335-0381-1) | Feb 9, 2022 |
| 71335-0381-2 | 90 TABLET in 1 BOTTLE (71335-0381-2) | Feb 9, 2022 |
| 71335-0381-3 | 60 TABLET in 1 BOTTLE (71335-0381-3) | Feb 9, 2022 |
| 71335-0381-4 | 28 TABLET in 1 BOTTLE (71335-0381-4) | Feb 9, 2022 |
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