Ramipril
- Product NDC
- 72789-415
- 11-digit product format
- 727890415
- Labeler code
- 72789
- Product ID
- 72789-415_41232435-0741-f3f6-e063-6294a90a9378
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ramipril
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Application
- ANDA078832
- Marketing category
- ANDA
- Marketing start
- 2010-11-20
- Substance
- RAMIPRIL
- Active strength
- 2.5 mg/1
- Pharmacologic classes
- Angiotensin Converting Enzyme Inhibitor [EPC], Angiotensin-converting Enzyme Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| L35JN3I7SJ | RAMIPRIL | 87333-19-5 | RAMIPRIL |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 72789-415-90 | 72789041590 | 90 CAPSULE in 1 BOTTLE, PLASTIC (72789-415-90) | 90 capsule | 2024-06-21 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Ramipril | PD-Rx Pharmaceuticals, Inc. | 2025-10-14 | HUMAN PRESCRIPTION DRUG LABEL | 18 |
| Ramipril | PD-Rx Pharmaceuticals, Inc. | 2024-06-21 | HUMAN PRESCRIPTION DRUG LABEL | 17 |