Ramipril
- Product NDC
- 50090-7887
- 11-digit product format
- 500907887
- Labeler code
- 50090
- Product ID
- 50090-7887_35bb8a56-019a-43f0-b0d7-f8ec7ed1fb4b
- 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
- 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
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Ramipril
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| RAMIPRIL | 10 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | L35JN3I7SJ |
| Rxcui | 261962 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 50090-7887-0 | Ramipril | 90 in 1 BOTTLE | CAPSULE | 90 | | 8 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 50090-7887-0 | 50090788700 | 90 CAPSULE in 1 BOTTLE (50090-7887-0) | 90 capsule | 2026-02-06 | No | No | Historical |