NDC 63629-3739 – Lisinopril and Hydrochlorothiazide
Hydrochlorothiazide 25 mg/1; Lisinopril 20 mg/1 · Tablet · Oral
Product NDC63629-3739
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 25 mg/1
- Lisinopril 20 mg/1
Uses, dosage, side effects and warnings for Lisinopril and Hydrochlorothiazide →
Package NDC codes (6)
| Package NDC | Description | Since |
|---|---|---|
| 63629-3739-1 | 30 TABLET in 1 BOTTLE (63629-3739-1) | Jun 26, 2008 |
| 63629-3739-2 | 60 TABLET in 1 BOTTLE (63629-3739-2) | Oct 6, 2011 |
| 63629-3739-3 | 90 TABLET in 1 BOTTLE (63629-3739-3) | Oct 21, 2010 |
| 63629-3739-4 | 120 TABLET in 1 BOTTLE (63629-3739-4) | Dec 22, 2021 |
| 63629-3739-5 | 100 TABLET in 1 BOTTLE (63629-3739-5) | May 11, 2018 |
| 63629-3739-6 | 180 TABLET in 1 BOTTLE (63629-3739-6) | Dec 22, 2021 |
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