FEIBA
- Product NDC
- 64193-424
- 11-digit product format
- 641930424
- Labeler code
- 64193
- Product ID
- 64193-424_30be11d8-bb0b-4f10-8ef6-be656d679390
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- anti-inhibitor coagulant complex
- Dosage form
- KIT
- Labeler
- Takeda Pharmaceuticals America, Inc.
- Application
- BLA101447
- Marketing category
- BLA
- Marketing start
- 1986-01-31
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- FEIBA
- Listing expiration
- 2026-12-31
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Rxcui | 1659998, 1660001 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 64193-324-01 | FEIBA | 20 mL in 1 VIAL, GLASS | POWDER, FOR SOLUTION | 20 mL | 1000 U in 20mL | 30 |
| 64193-424-02 | FEIBA | 1 in 1 CARTON | KIT | 1 | | 30 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 64193-424 | FEIBA (ANTI-INHIBITOR COAGULANT COMPLEX) KIT [TAKEDA PHARMACEUTICALS AMERICA, INC.] | 29 | Current NDC, Legacy NDC, 2 package rows | 20250109_752604e5-4ea2-44f4-83ed-1569373f6412.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 64193-324-01 | 64193032401 | 20 mL in 1 VIAL, GLASS | 20 ml | | | | | Historical |
| 64193-424-02 | 64193042402 | 1 KIT in 1 CARTON (64193-424-02) * 20 mL in 1 VIAL, GLASS (64193-324-01) * 20 mL in 1 VIAL, GLASS (64764-517-20) | 1 kit | 1986-01-31 | 0000-00-00 | No | No | Current |