NDC 69097-971 – Lisinopril and Hydrochlorothiazide
Lisinopril 20 mg/1; Hydrochlorothiazide 25 mg/1 · Tablet · Oral
Product NDC69097-971
Product details
- Brand name
- Lisinopril and Hydrochlorothiazide
- Generic name
- Lisinopril and Hydrochlorothiazide Tablets
- Labeler
- Cipla USA Inc.
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA204058
- Marketed since
- December 26, 2019
- Listing expires
- December 31, 2026
- 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 (4)
| Package NDC | Description | Since |
|---|---|---|
| 69097-971-05 | 90 TABLET in 1 BOTTLE (69097-971-05) | Dec 26, 2019 |
| 69097-971-07 | 100 TABLET in 1 BOTTLE (69097-971-07) | Dec 26, 2019 |
| 69097-971-12 | 500 TABLET in 1 BOTTLE (69097-971-12) | Dec 26, 2019 |
| 69097-971-15 | 1000 TABLET in 1 BOTTLE (69097-971-15) | Dec 26, 2019 |
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