NDC 65862-045 – Lisinopril and Hydrochlorothiazide
Lisinopril 20 mg/1; Hydrochlorothiazide 25 mg/1 · Tablet · Oral
Product NDC65862-045
Product details
- Brand name
- Lisinopril and Hydrochlorothiazide
- Generic name
- Lisinopril and Hydrochlorothiazide
- Labeler
- Aurobindo Pharma Limited
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA077606
- Marketed since
- March 14, 2006
- Listing expires
- December 31, 2027
- Pharmacologic class
- Angiotensin Converting Enzyme Inhibitor; Thiazide Diuretic
Active ingredients
- Lisinopril 20 mg/1
- Hydrochlorothiazide 25 mg/1
Uses, dosage, side effects and warnings for Lisinopril and Hydrochlorothiazide →
Package NDC codes (5)
| Package NDC | Description | Since |
|---|---|---|
| 65862-045-00 | 100 TABLET in 1 BOTTLE (65862-045-00) | Mar 14, 2006 |
| 65862-045-01 | 100 TABLET in 1 BOTTLE (65862-045-01) | Mar 14, 2006 |
| 65862-045-05 | 500 TABLET in 1 BOTTLE (65862-045-05) | Mar 14, 2006 |
| 65862-045-30 | 30 TABLET in 1 BOTTLE (65862-045-30) | Mar 14, 2006 |
| 65862-045-99 | 1000 TABLET in 1 BOTTLE (65862-045-99) | Mar 14, 2006 |
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