Enalapril Maleate
- Product NDC
- 71335-2608
- 11-digit product format
- 713352608
- Labeler code
- 71335
- Product ID
- 71335-2608_8a9ca091-53b5-44eb-b5dc-ec12d5b35f58
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Enalapril Maleate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA075657
- Marketing category
- ANDA
- Marketing start
- 2001-01-23
- Substance
- ENALAPRIL MALEATE
- Active strength
- 10 mg/1
- Pharmacologic classes
- Angiotensin Converting Enzyme Inhibitor [EPC], Angiotensin-converting Enzyme Inhibitors [MoA], Decreased Blood Pressure [PE]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Enalapril Maleate
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ENALAPRIL MALEATE | 10 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 9O25354EPJ |
| Rxcui | 858817 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 71335-2608-1 | 71335260801 | 60 TABLET in 1 BOTTLE (71335-2608-1) | 60 tablet | 2026-03-06 | No | No | Historical |
| 71335-2608-2 | 71335260802 | 30 TABLET in 1 BOTTLE (71335-2608-2) | 30 tablet | 2026-03-06 | No | No | Historical |
| 71335-2608-3 | 71335260803 | 100 TABLET in 1 BOTTLE (71335-2608-3) | 100 tablet | 2026-03-06 | No | No | Historical |
| 71335-2608-4 | 71335260804 | 90 TABLET in 1 BOTTLE (71335-2608-4) | 90 tablet | 2026-03-06 | No | No | Historical |
| 71335-2608-5 | 71335260805 | 120 TABLET in 1 BOTTLE (71335-2608-5) | 120 tablet | 2026-03-06 | No | No | Historical |