Brinsupri
- Product NDC
- 71558-002
- 11-digit product format
- 715580002
- Labeler code
- 71558
- Product ID
- 71558-002_43046e5b-e40b-423d-a98d-a2fecc2cbd2e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Brensocatib
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Insmed Incorporated
- Application
- NDA217673
- Marketing category
- NDA
- Marketing start
- 2025-08-12
- Substance
- BRENSOCATIB
- Active strength
- 25 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Brinsupri
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| BRENSOCATIB | 25 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 25CG88L0BB |
| Rxcui | 2721885, 2721891, 2721893, 2721895 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 71558-002-30 | Brinsupri | 30 in 1 BOTTLE | TABLET | 30 | | 3 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 71558-002-30 | 71558000230 | 30 TABLET in 1 BOTTLE (71558-002-30) | 30 tablet | 2025-08-12 | No | No | Historical |