ENALAPRIL MALEATE
- Product NDC
- 50436-4353
- 11-digit product format
- 504364353
- Labeler code
- 50436
- Product ID
- 50436-4353_b2536193-1c24-4156-b6ec-c45e66359d9c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- ENALAPRIL MALEATE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Unit Dose Services
- Application
- ANDA075483
- Marketing category
- ANDA
- Marketing start
- 2009-12-11
- Marketing end
- 0000-00-00
- Substance
- ENALAPRIL MALEATE
- Active strength
- 3 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
- 2019-12-31
- 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 |
|---|
| 50436-4353-1 | ENALAPRIL MALEATE | 30 in 1 BOTTLE | TABLET | 30 | | 2 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50436-4353 | ENALAPRIL MALEATE TABLET [UNIT DOSE SERVICES] | 2 | Legacy NDC, 1 package rows | 20130517_0fff54ec-d45e-4938-9131-c5abea57c0b4.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 50436-4353-1 | 50436435301 | 30 in 1 BOTTLE | Historical |