NDC 70518-0174 – Lisinopril and Hydrochlorothiazide
Hydrochlorothiazide 25 mg/1; Lisinopril 20 mg/1 · Tablet · Oral
Product NDC70518-0174
Product details
- Brand name
- Lisinopril and Hydrochlorothiazide
- Generic name
- Lisinopril and Hydrochlorothiazide
- Labeler
- REMEDYREPACK INC.
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA077912
- Marketed since
- January 23, 2017
- 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 (4)
| Package NDC | Description | Since |
|---|---|---|
| 70518-0174-0 | 30 TABLET in 1 BOTTLE, PLASTIC (70518-0174-0) | Jan 23, 2017 |
| 70518-0174-1 | 90 TABLET in 1 BOTTLE, PLASTIC (70518-0174-1) | Feb 2, 2017 |
| 70518-0174-2 | 100 TABLET in 1 BOTTLE, PLASTIC (70518-0174-2) | May 4, 2017 |
| 70518-0174-3 | 30 TABLET in 1 BLISTER PACK (70518-0174-3) | Mar 6, 2018 |
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