NDC 30698-453 – Lotensin HCT
Benazepril Hydrochloride 20 mg/1; Hydrochlorothiazide 12.5 mg/1 · Tablet · Oral
Product NDC30698-453
Product details
- Brand name
- Lotensin HCT
- Generic name
- benazepril hydrochloride and hydrochlorothiazide
- Labeler
- Validus Pharmaceuticals LLC
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- NDA · NDA020033
- Marketed since
- May 30, 1992
- Listing expires
- December 31, 2027
- Pharmacologic class
- Angiotensin Converting Enzyme Inhibitor; Thiazide Diuretic
Active ingredients
- Benazepril Hydrochloride 20 mg/1
- Hydrochlorothiazide 12.5 mg/1
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 30698-453-01 | 100 TABLET in 1 BOTTLE (30698-453-01) | May 30, 1992 |