NDC 63629-4470 – Lisinopril and Hydrochlorothiazide
Hydrochlorothiazide 12.5 mg/1; Lisinopril 20 mg/1 · Tablet · Oral
Product NDC63629-4470
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 20 mg/1
Uses, dosage, side effects and warnings for Lisinopril and Hydrochlorothiazide →
Package NDC codes (6)
| Package NDC | Description | Since |
|---|---|---|
| 63629-4470-1 | 30 TABLET in 1 BOTTLE (63629-4470-1) | Mar 24, 2011 |
| 63629-4470-2 | 90 TABLET in 1 BOTTLE (63629-4470-2) | May 16, 2011 |
| 63629-4470-3 | 100 TABLET in 1 BOTTLE (63629-4470-3) | Dec 22, 2021 |
| 63629-4470-4 | 60 TABLET in 1 BOTTLE (63629-4470-4) | Feb 10, 2015 |
| 63629-4470-5 | 360 TABLET in 1 BOTTLE (63629-4470-5) | Dec 22, 2021 |
| 63629-4470-6 | 4 TABLET in 1 BOTTLE (63629-4470-6) | Dec 22, 2021 |
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