Lisinopril and Hydrochlorothiazide
- Product NDC
- 71335-0576
- 11-digit product format
- 713350576
- Labeler code
- 71335
- Product ID
- 71335-0576_1b436520-90f8-487b-97dc-cd2544b7aeed
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Lisinopril and Hydrochlorothiazide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA076262
- Marketing category
- ANDA
- Marketing start
- 2002-07-02
- Marketing end
- 0000-00-00
- Substance
- LISINOPRIL; HYDROCHLOROTHIAZIDE
- Active strength
- 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
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71335-0576-1 | 71335057601 | 30 TABLET in 1 BOTTLE (71335-0576-1) | 30 tablet | 2015-08-10 | 0000-00-00 | No | No | Current |
| 71335-0576-2 | 71335057602 | 90 TABLET in 1 BOTTLE (71335-0576-2) | 90 tablet | 2015-08-10 | 0000-00-00 | No | No | Current |
| 71335-0576-3 | 71335057603 | 180 TABLET in 1 BOTTLE (71335-0576-3) | 180 tablet | 2015-08-10 | 0000-00-00 | No | No | Current |