Lisinopril and Hydrochlorothiazide
- Product NDC
- 71335-9730
- 11-digit product format
- 713359730
- Labeler code
- 71335
- Product ID
- 71335-9730_17a2b36c-22c3-43cf-8dc0-87852dd5fe94
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Lisinopril and Hydrochlorothiazide Tablets
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA076230
- Marketing category
- ANDA
- Marketing start
- 2015-03-12
- Substance
- HYDROCHLOROTHIAZIDE; LISINOPRIL
- Active strength
- 12.5; 20 mg/1; mg/1
- Pharmacologic classes
- Angiotensin Converting Enzyme Inhibitor [EPC], Angiotensin-converting Enzyme Inhibitors [MoA], Increased Diuresis [PE], Thiazide Diuretic [EPC], Thiazides [CS]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 0J48LPH2TH | HYDROCHLOROTHIAZIDE | 58-93-5 | HYDROCHLOROTHIAZIDE |
| E7199S1YWR | LISINOPRIL | 83915-83-7 | LISINOPRIL |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 71335-9730-1 | 71335973001 | 30 TABLET in 1 BOTTLE (71335-9730-1) | 30 tablet | 2023-06-22 | No | No | Historical |
| 71335-9730-2 | 71335973002 | 90 TABLET in 1 BOTTLE (71335-9730-2) | 90 tablet | 2023-06-22 | No | No | Historical |
| 71335-9730-3 | 71335973003 | 100 TABLET in 1 BOTTLE (71335-9730-3) | 100 tablet | 2023-06-22 | No | No | Historical |
| 71335-9730-4 | 71335973004 | 60 TABLET in 1 BOTTLE (71335-9730-4) | 60 tablet | 2023-06-22 | No | No | Historical |
| 71335-9730-5 | 71335973005 | 360 TABLET in 1 BOTTLE (71335-9730-5) | 360 tablet | 2023-06-22 | No | No | Historical |
| 71335-9730-6 | 71335973006 | 4 TABLET in 1 BOTTLE (71335-9730-6) | 4 tablet | 2023-06-22 | No | No | Historical |