ENALAPRIL MALEATE
- Product NDC
- 60760-226
- 11-digit product format
- 607600226
- Labeler code
- 60760
- Product ID
- 60760-226_f06e8f22-b76e-f8fa-e053-2a95a90a8e2d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- ENALAPRIL MALEATE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- St Marys Medical Park Pharmacy
- Application
- ANDA075483
- Marketing category
- ANDA
- Marketing start
- 2014-04-21
- 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
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 60760-226 | ENALAPRIL MALEATE TABLET [ST MARYS MEDICAL PARK PHARMACY] | 10 | Legacy NDC | 20221223_f84ea753-631f-4f13-a17b-26c38ddaac3b.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 60760-226-30 | 60760022630 | 30 TABLET in 1 BOTTLE, PLASTIC (60760-226-30) | 30 tablet | 2014-04-21 | 0000-00-00 | No | No | Current |