Helixate FS
- Product NDC
- 0053-8132
- 11-digit product format
- 000538132
- Labeler code
- 0053
- Product ID
- 0053-8132_a8999296-44d4-427a-a82d-d23a0c622e71
- Type
- PLASMA DERIVATIVE
- Nonproprietary name
- Antihemophilic Factor, Recombinant
- Dosage form
- KIT
- Labeler
- CSL Behring LLC
- Application
- BLA103332
- Marketing category
- BLA
- Marketing start
- 2000-08-18
- Marketing end
- 0000-00-00
- Active strength
- 0
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 0053-8132-02 | EA - Each | 0053-8132 | 24fc8511-455e-4eff-9ce5-df4dfe0f203b | 1 | 2012-07-24 |