NDC 71335-0862 – Lisinopril and Hydrochlorothiazide
Lisinopril 20 mg/1; Hydrochlorothiazide 12.5 mg/1 · Tablet · Oral
Product NDC71335-0862
Product details
- Brand name
- Lisinopril and Hydrochlorothiazide
- Generic name
- Lisinopril and Hydrochlorothiazide
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA076194
- Marketed since
- March 4, 2003
- Listing expires
- December 31, 2026
- Pharmacologic class
- Angiotensin Converting Enzyme Inhibitor; Thiazide Diuretic
Active ingredients
- Lisinopril 20 mg/1
- Hydrochlorothiazide 12.5 mg/1
Uses, dosage, side effects and warnings for Lisinopril and Hydrochlorothiazide →
Package NDC codes (6)
| Package NDC | Description | Since |
|---|---|---|
| 71335-0862-1 | 30 TABLET in 1 BOTTLE (71335-0862-1) | Feb 9, 2022 |
| 71335-0862-2 | 90 TABLET in 1 BOTTLE (71335-0862-2) | Feb 9, 2022 |
| 71335-0862-3 | 100 TABLET in 1 BOTTLE (71335-0862-3) | Feb 9, 2022 |
| 71335-0862-4 | 60 TABLET in 1 BOTTLE (71335-0862-4) | Feb 9, 2022 |
| 71335-0862-5 | 360 TABLET in 1 BOTTLE (71335-0862-5) | Feb 9, 2022 |
| 71335-0862-6 | 4 TABLET in 1 BOTTLE (71335-0862-6) | Feb 9, 2022 |
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