ANASCORP is a Intravenous Injection, Powder, Lyophilized, For Solution in the Plasma Derivative category. It is labeled and distributed by Rare Disease Therapeutics, Inc. The primary component is Centruroides Fab2 Antivenin (equine).
| Product ID | 66621-0150_036723fb-cef3-4705-b9c5-ad61049acef5 |
| NDC | 66621-0150 |
| Product Type | Plasma Derivative |
| Proprietary Name | ANASCORP |
| Generic Name | Centruroides (scorpion) Immune F(ab)2 (equine) |
| Dosage Form | Injection, Powder, Lyophilized, For Solution |
| Route of Administration | INTRAVENOUS |
| Marketing Start Date | 2011-08-03 |
| Marketing Category | BLA / BLA |
| Application Number | BLA125335 |
| Labeler Name | Rare Disease Therapeutics, Inc |
| Substance Name | CENTRUROIDES FAB2 ANTIVENIN (EQUINE) |
| Active Ingredient Strength | 7 mg/mL |
| Pharm Classes | Antivenin [EPC], Antivenins [CS], Passively Acquired Immunity [PE], Venom Neutralization [MoA] |
| NDC Exclude Flag | N |
| Listing Certified Through | 2023-12-31 |
| Marketing Start Date | 2011-08-03 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | BLA |
| Application Number | BLA125335 |
| Product Type | PLASMA DERIVATIVE |
| Billing Unit | EA |
| Marketing Start Date | 2017-06-27 |
| Marketing Category | BLA |
| Application Number | BLA125335 |
| Product Type | PLASMA DERIVATIVE |
| Billing Unit | EA |
| Marketing Start Date | 2011-08-03 |
| Ingredient | Strength |
|---|---|
| CENTRUROIDES FAB2 ANTIVENIN (EQUINE) | 3.8 mg/mL |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() ANASCORP 78825607 3403334 Live/Registered |
LABORATORIOS SILANES, S.A. DE C.V. 2006-02-28 |
![]() ANASCORP 78295395 not registered Dead/Abandoned |
Pharmasil, Inc. 2003-09-03 |
![]() ANASCORP 76213985 not registered Dead/Abandoned |
Orphan Pharmaceuticals, U.S.A., Inc. 2001-02-21 |