Enalapril Maleate and Hydrochlorothiazide
- Product NDC
- 0713-1052
- 11-digit product format
- 007131052
- Labeler code
- 0713
- Product ID
- 0713-1052_69ffa251-a09c-4766-8c11-1a006e1a8b97
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Enalapril Maleate and Hydrochlorothiazide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Cosette Pharmaceuticals, Inc.
- Application
- ANDA075727
- Marketing category
- ANDA
- Marketing start
- 2016-03-31
- Marketing end
- 0000-00-00
- Substance
- ENALAPRIL MALEATE; HYDROCHLOROTHIAZIDE
- Active strength
- 10 mg/1; mg/1
- Pharmacologic classes
- Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA],Decreased Blood Pressure [PE],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 |
|---|
| 0713-1052-01 | 00713105201 | 100 TABLET in 1 BOTTLE (0713-1052-01) | 100 tablet | 2016-03-31 | 0000-00-00 | No | No | Current |