Ramipril
- Product NDC
- 68071-3971
- 11-digit product format
- 680713971
- Labeler code
- 68071
- Product ID
- 68071-3971_4bd2d524-50ef-b1a0-e063-6294a90a78cb
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ramipril
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals, Inc.
- Application
- ANDA091604
- Marketing category
- ANDA
- Marketing start
- 2011-06-08
- Substance
- RAMIPRIL
- Active strength
- 10 mg/1
- Pharmacologic classes
- Angiotensin Converting Enzyme Inhibitor [EPC], Angiotensin-converting Enzyme Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- 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 |
|---|
| 68071-3971-3 | 68071397103 | 30 CAPSULE in 1 BOTTLE (68071-3971-3) | 30 capsule | 2026-02-27 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Ramipril | NuCare Pharmaceuticals, Inc. | 2026-02-27 | HUMAN PRESCRIPTION DRUG LABEL | 1 |