Ramipril
- Product NDC
- 71205-029
- 11-digit product format
- 712050029
- Labeler code
- 71205
- Product ID
- 71205-029_5e9007b1-3052-4e46-b4e3-28174e3efdfd
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ramipril
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Proficient Rx LP
- 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
- 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 |
|---|
| 71205-029-30 | 71205002930 | 30 CAPSULE in 1 BOTTLE (71205-029-30) | 30 capsule | 2018-05-01 | No | No | Historical |
| 71205-029-60 | 71205002960 | 60 CAPSULE in 1 BOTTLE (71205-029-60) | 60 capsule | 2018-05-01 | No | No | Historical |
| 71205-029-90 | 71205002990 | 90 CAPSULE in 1 BOTTLE (71205-029-90) | 90 capsule | 2018-05-01 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Ramipril | Proficient Rx LP | 2019-10-01 | HUMAN PRESCRIPTION DRUG LABEL | 3 |