Ramipril
- Product NDC
- 50090-5947
- 11-digit product format
- 500905947
- Labeler code
- 50090
- Product ID
- 50090-5947_cbeb0bac-dd52-41a4-8d12-ead3f80118f0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ramipril
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- 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
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| L35JN3I7SJ | RAMIPRIL | 87333-19-5 | RAMIPRIL |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-5947-0 | 50090594700 | 100 CAPSULE in 1 BOTTLE (50090-5947-0) | 100 capsule | 2022-03-24 | 0000-00-00 | No | No | Current |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Ramipril | A-S Medication Solutions | 2022-04-01 | Human Prescription Drug Label | 1 |