Enalapril Maleate
- Product NDC
- 60760-392
- 11-digit product format
- 607600392
- Labeler code
- 60760
- Product ID
- 60760-392_81a04c5e-55fe-339d-e053-2a91aa0a9a4d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Enalapril Maleate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- St. Mary's Medical Park Pharmacy
- Application
- NDA018998
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2019-02-11
- 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
- 2020-12-31
- 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 |
|---|
| 60760-392-30 | 60760039230 | 30 TABLET in 1 BOTTLE, PLASTIC (60760-392-30) | 30 tablet | 2019-02-11 | 0000-00-00 | No | No | Current |