Enalapril Maleate
- Product NDC
- 51138-036
- 11-digit product format
- 511380036
- Labeler code
- 51138
- Product ID
- 51138-036_e983ec9b-9e09-4bc6-9225-0d3a6dc77008
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Enalapril Maleate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Med Health Pharma, LLC
- Application
- ANDA075483
- Marketing category
- ANDA
- Marketing start
- 2011-01-01
- Marketing end
- 0000-00-00
- Substance
- ENALAPRIL MALEATE
- Active strength
- 20 mg/1
- Pharmacologic classes
- Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA],Decreased Blood Pressure [PE]
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 51138-036-30 | Enalapril Maleate | 30 in 1 BOTTLE | TABLET | 30 | | 1 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 51138-036 | ENALAPRIL MALEATE TABLET [MED HEALTH PHARMA, LLC] | 1 | Legacy NDC, 1 package rows | 20110103_d59a23ba-9e28-42a3-8bfe-a3742fdfdebe.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 51138-036-30 | 51138003630 | 30 in 1 BOTTLE | Historical |