Ramipril
- Product NDC
- 51655-406
- 11-digit product format
- 516550406
- Labeler code
- 51655
- Product ID
- 51655-406_48fef521-1b1f-d0d5-e063-6394a90ac7b1
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ramipril
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Northwind Health Company, LLC
- Application
- ANDA091604
- Marketing category
- ANDA
- Marketing start
- 2022-09-06
- 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 |
|---|
| 51655-406-52 | Ramipril | 30 in 1 BOTTLE, PLASTIC | CAPSULE | 30 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 51655-406 | RAMIPRIL CAPSULE [NORTHWIND PHARMACEUTICALS, LLC] | 1 | Current NDC, 1 package rows | 20230328_f2f325b8-f33d-3b93-e053-2995a90aa660.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 51655-406-52 | 51655040652 | 30 CAPSULE in 1 BOTTLE, PLASTIC (51655-406-52) | 30 capsule | 2022-09-06 | No | No | Current |