Dabigatran Etexilate
- Product NDC
- 50090-7656
- 11-digit product format
- 500907656
- Labeler code
- 50090
- Product ID
- 50090-7656_c9ac120f-f8a2-4be5-9060-4f90a2e1ef10
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Dabigatran Etexilate
- Dosage form
- CAPSULE, COATED PELLETS
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA208040
- Marketing category
- ANDA
- Marketing start
- 2022-06-20
- Substance
- DABIGATRAN ETEXILATE MESYLATE
- Active strength
- 75 mg/1
- Pharmacologic classes
- Direct Thrombin Inhibitor [EPC], Thrombin Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Dabigatran Etexilate
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| DABIGATRAN ETEXILATE MESYLATE | 75 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | SC7NUW5IIT |
| Rxcui | 1037179 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 50090-7656-0 | Dabigatran Etexilate | 60 in 1 BOTTLE | CAPSULE, COATED PELLETS | 60 | | 1 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 50090-7656-0 | 50090765600 | 60 CAPSULE, COATED PELLETS in 1 BOTTLE (50090-7656-0) | 2025-09-18 | No | No | Current |