Ramipril
- Product NDC
- 68788-7008
- 11-digit product format
- 687887008
- Labeler code
- 68788
- Product ID
- 68788-7008_01112b3d-1378-4cc7-8a37-5f1bf6e71d12
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ramipril
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA091604
- Marketing category
- ANDA
- Marketing start
- 2017-08-17
- Marketing end
- 0000-00-00
- Substance
- RAMIPRIL
- Active strength
- 5 mg/1
- Pharmacologic classes
- Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| L35JN3I7SJ | RAMIPRIL | 87333-19-5 | RAMIPRIL |