Ramipril
- Product NDC
- 70518-1200
- 11-digit product format
- 705181200
- Labeler code
- 70518
- Product ID
- 70518-1200_e3275fcc-4f2e-f54a-e053-2a95a90a737f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ramipril
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA091604
- Marketing category
- ANDA
- Marketing start
- 2018-05-15
- Marketing end
- 0000-00-00
- 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
- 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 |
|---|
| 70518-1200-0 | 70518120000 | 90 CAPSULE in 1 BOTTLE, PLASTIC (70518-1200-0) | 90 capsule | 2018-05-15 | 0000-00-00 | No | No | Current |