NDC 68071-4435 – Lisinopril and Hydrochlorothiazide
Lisinopril 20 mg/1; Hydrochlorothiazide 12.5 mg/1 · Tablet · Oral
Product NDC68071-4435
Product details
- Brand name
- Lisinopril and Hydrochlorothiazide
- Generic name
- Lisinopril and Hydrochlorothiazide
- Labeler
- NuCare Pharmaceuticals,Inc.
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA076194
- Marketed since
- March 4, 2003
- Listing expires
- December 31, 2026
- Pharmacologic class
- Angiotensin Converting Enzyme Inhibitor; Thiazide Diuretic
Active ingredients
- Lisinopril 20 mg/1
- Hydrochlorothiazide 12.5 mg/1
Uses, dosage, side effects and warnings for Lisinopril and Hydrochlorothiazide →
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 68071-4435-3 | 30 TABLET in 1 BOTTLE (68071-4435-3) | May 16, 2018 |
| 68071-4435-6 | 60 TABLET in 1 BOTTLE (68071-4435-6) | May 16, 2018 |
| 68071-4435-9 | 90 TABLET in 1 BOTTLE (68071-4435-9) | May 16, 2018 |
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