NDC 71335-0479 – Lisinopril and Hydrochlorothiazide
Hydrochlorothiazide 12.5 mg/1; Lisinopril 10 mg/1 · Tablet · Oral
Product NDC71335-0479
Product details
- Brand name
- Lisinopril and Hydrochlorothiazide
- Generic name
- Lisinopril and Hydrochlorothiazide
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA077912
- Marketed since
- October 4, 2006
- Listing expires
- December 31, 2027
- Pharmacologic class
- Angiotensin Converting Enzyme Inhibitor; Thiazide Diuretic
Active ingredients
- Hydrochlorothiazide 12.5 mg/1
- Lisinopril 10 mg/1
Uses, dosage, side effects and warnings for Lisinopril and Hydrochlorothiazide →
Package NDC codes (5)
| Package NDC | Description | Since |
|---|---|---|
| 71335-0479-1 | 90 TABLET in 1 BOTTLE (71335-0479-1) | Nov 23, 2021 |
| 71335-0479-2 | 60 TABLET in 1 BOTTLE (71335-0479-2) | Apr 3, 2024 |
| 71335-0479-3 | 30 TABLET in 1 BOTTLE (71335-0479-3) | Feb 25, 2022 |
| 71335-0479-4 | 100 TABLET in 1 BOTTLE (71335-0479-4) | Apr 3, 2024 |
| 71335-0479-5 | 120 TABLET in 1 BOTTLE (71335-0479-5) | Apr 3, 2024 |
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