NDC 69097-972 – Fosinopril Sodium and Hydrochlorothiazide
Fosinopril Sodium 10 mg/1; Hydrochlorothiazide 12.5 mg/1 · Tablet · Oral
Product NDC69097-972
Product details
- Brand name
- Fosinopril Sodium and Hydrochlorothiazide
- Generic name
- Fosinopril Sodium and Hydrochlorothiazide
- Labeler
- CIPLA USA INC.
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA090228
- Marketed since
- July 24, 2020
- Listing expires
- December 31, 2026
- Pharmacologic class
- Angiotensin Converting Enzyme Inhibitor; Thiazide Diuretic
Active ingredients
- Fosinopril Sodium 10 mg/1
- Hydrochlorothiazide 12.5 mg/1
Uses, dosage, side effects and warnings for Fosinopril Sodium and Hydrochlorothiazide →
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 69097-972-07 | 100 TABLET in 1 BOTTLE (69097-972-07) | Jul 24, 2020 |