NDC 71335-2091 – Lisinopril and Hydrochlorothiazide
Lisinopril 20 mg/1; Hydrochlorothiazide 25 mg/1 · Tablet · Oral
Product NDC71335-2091
Product details
- Brand name
- Lisinopril and Hydrochlorothiazide
- Generic name
- Lisinopril and Hydrochlorothiazide Tablets
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA076230
- Marketed since
- March 12, 2015
- Listing expires
- December 31, 2026
- Pharmacologic class
- Angiotensin Converting Enzyme Inhibitor; Thiazide Diuretic
Active ingredients
- Lisinopril 20 mg/1
- Hydrochlorothiazide 25 mg/1
Uses, dosage, side effects and warnings for Lisinopril and Hydrochlorothiazide →
Package NDC codes (6)
| Package NDC | Description | Since |
|---|---|---|
| 71335-2091-1 | 30 TABLET in 1 BOTTLE (71335-2091-1) | May 17, 2022 |
| 71335-2091-2 | 60 TABLET in 1 BOTTLE (71335-2091-2) | May 17, 2022 |
| 71335-2091-3 | 90 TABLET in 1 BOTTLE (71335-2091-3) | May 17, 2022 |
| 71335-2091-4 | 120 TABLET in 1 BOTTLE (71335-2091-4) | May 17, 2022 |
| 71335-2091-5 | 100 TABLET in 1 BOTTLE (71335-2091-5) | May 17, 2022 |
| 71335-2091-6 | 180 TABLET in 1 BOTTLE (71335-2091-6) | May 17, 2022 |
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