Ramipril
- Product NDC
- 63187-503
- 11-digit product format
- 631870503
- Labeler code
- 63187
- Product ID
- 63187-503_ae0002cb-15af-494b-bce9-2a31df064c4d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ramipril
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA077626
- Marketing category
- ANDA
- Marketing start
- 2008-06-10
- 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
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63187-503-30 | 63187050330 | 30 CAPSULE in 1 BOTTLE (63187-503-30) | 30 capsule | 2014-06-01 | 0000-00-00 | No | No | Current |
| 63187-503-60 | 63187050360 | 60 CAPSULE in 1 BOTTLE (63187-503-60) | 60 capsule | 2014-06-01 | 0000-00-00 | No | No | Current |
| 63187-503-90 | 63187050390 | 90 CAPSULE in 1 BOTTLE (63187-503-90) | 90 capsule | 2014-06-01 | 0000-00-00 | No | No | Current |