This brand name is authorized in United States.
The drug BAT contains a combination of these active pharmaceutical ingredients (APIs):
1
|
UNII
LE3J6I6DXP - EQUINE BOTULINUM NEUROTOXIN A IMMUNE FAB2
|
2
|
UNII
VSK09VP4HL - EQUINE BOTULINUM NEUROTOXIN B IMMUNE FAB2
|
3
|
UNII
X5I2P7E9TY - EQUINE BOTULINUM NEUROTOXIN C IMMUNE FAB2
|
4
|
UNII
30Y9N0SEBE - EQUINE BOTULINUM NEUROTOXIN D IMMUNE FAB2
|
5
|
UNII
T95649SUV7 - EQUINE BOTULINUM NEUROTOXIN E IMMUNE FAB2
|
6
|
UNII
RJN8G983LQ - EQUINE BOTULINUM NEUROTOXIN F IMMUNE FAB2
|
7
|
UNII
943578J0XG - EQUINE BOTULINUM NEUROTOXIN G IMMUNE FAB2
|
This drug has been assigned below unique identifiers within the countries it is being marketed:
Country | Identification scheme | Identifier(s) |
---|---|---|
US | FDA, National Drug Code | 60492-0075 |
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