Enalapril Maleate
- Product NDC
- 70518-1664
- 11-digit product format
- 705181664
- Labeler code
- 70518
- Product ID
- 70518-1664_e5bfab02-560d-2069-e053-2995a90af53c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Enalapril Maleate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA075657
- Marketing category
- ANDA
- Marketing start
- 2018-11-12
- Marketing end
- 0000-00-00
- 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
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70518-1664 | ENALAPRIL MALEATE TABLET [REMEDYREPACK INC.] | 9 | Legacy NDC | 20240224_246e0ed0-f8ca-483b-a1ce-91052f3f35f0.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-1664-0 | 70518166400 | 30 TABLET in 1 BLISTER PACK (70518-1664-0) | 30 tablet | 2018-11-12 | 0000-00-00 | No | No | Current |