NDC 68788-8253 – Lisinopril and Hydrochlorothiazide
Lisinopril 20 mg/1; Hydrochlorothiazide 12.5 mg/1 · Tablet · Oral
Product NDC68788-8253
Product details
- Brand name
- Lisinopril and Hydrochlorothiazide
- Generic name
- Lisinopril and Hydrochlorothiazide Tablets
- Labeler
- Preferred Pharmaceuticals Inc.
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA076230
- Marketed since
- October 1, 2022
- Listing expires
- December 31, 2027
- 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 (4)
| Package NDC | Description | Since |
|---|---|---|
| 68788-8253-1 | 100 TABLET in 1 BOTTLE (68788-8253-1) | Oct 1, 2022 |
| 68788-8253-3 | 30 TABLET in 1 BOTTLE (68788-8253-3) | Oct 1, 2022 |
| 68788-8253-6 | 60 TABLET in 1 BOTTLE (68788-8253-6) | Oct 1, 2022 |
| 68788-8253-9 | 90 TABLET in 1 BOTTLE (68788-8253-9) | Oct 1, 2022 |
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