Ramipril
- Product NDC
- 63629-7260
- 11-digit product format
- 636297260
- Labeler code
- 63629
- Product ID
- 63629-7260_5d42a08f-068a-41a5-90a9-0f1585eb5418
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ramipril
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA091604
- Marketing category
- ANDA
- Marketing start
- 2011-06-08
- Marketing end
- 0000-00-00
- Substance
- RAMIPRIL
- Active strength
- 3 mg/1
- Pharmacologic classes
- Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| L35JN3I7SJ | RAMIPRIL | 87333-19-5 | RAMIPRIL |