Ramipril
- Product NDC
- 50090-4691
- 11-digit product format
- 500904691
- Labeler code
- 50090
- Product ID
- 50090-4691_76ac5599-12ce-4558-be15-737ba0d7d907
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ramipril
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA077626
- Marketing category
- ANDA
- Marketing start
- 2008-06-10
- 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
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-4691-0 | 50090469100 | 30 CAPSULE in 1 BOTTLE (50090-4691-0) | 30 capsule | 2019-11-06 | 0000-00-00 | No | No | Current |
| 50090-4691-1 | 50090469101 | 90 CAPSULE in 1 BOTTLE (50090-4691-1) | 90 capsule | 2019-11-06 | 0000-00-00 | No | No | Current |