RAMIPRIL
- Product NDC
- 61919-833
- 11-digit product format
- 619190833
- Labeler code
- 61919
- Product ID
- 61919-833_2b5cc18d-4342-40dd-e054-00144ff88e88
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- RAMIPRIL
- Dosage form
- CAPSULE, GELATIN COATED
- Route
- ORAL
- Labeler
- DIRECT RX
- Application
- ANDA091604
- Marketing category
- ANDA
- Marketing start
- 2016-01-13
- 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
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| L35JN3I7SJ | RAMIPRIL | 87333-19-5 | RAMIPRIL |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| RAMIPRIL 10mg | DIRECT RX | 2016-02-09 | HUMAN PRESCRIPTION DRUG LABEL | 1 |