NDC 71610-838 – Lisinopril and Hydrochlorothiazide
Hydrochlorothiazide 12.5 mg/1; Lisinopril 20 mg/1 · Tablet · Oral
Product NDC71610-838
Product details
- Brand name
- Lisinopril and Hydrochlorothiazide
- Generic name
- Lisinopril and Hydrochlorothiazide
- Labeler
- Aphena Pharma Solutions - Tennessee, LLC
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA077912
- Marketed since
- October 4, 2006
- Listing expires
- December 31, 2026
- 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 (5)
| Package NDC | Description | Since |
|---|---|---|
| 71610-838-30 | 30 TABLET in 1 BOTTLE (71610-838-30) | May 31, 2024 |
| 71610-838-53 | 60 TABLET in 1 BOTTLE (71610-838-53) | May 31, 2024 |
| 71610-838-60 | 90 TABLET in 1 BOTTLE (71610-838-60) | May 31, 2024 |
| 71610-838-70 | 120 TABLET in 1 BOTTLE (71610-838-70) | May 31, 2024 |
| 71610-838-80 | 180 TABLET in 1 BOTTLE (71610-838-80) | May 31, 2024 |
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