BOTOX (Allergan, Inc.)
Welcome to the PulseAid listing for the BOTOX drug offered from Allergan, Inc.. This Acetylcholine Release Inhibitor [EPC],Acetylcholine Release Inhibitors [MoA] pharmaceutical is classified as a HUMAN PRESCRIPTION DRUG. Below, you can view details for this drug, such as its dosage form, route of delivery, start market/end market dates, and more. We have also randomly listed additional pharmaceuticals used in the same HUMAN PRESCRIPTION DRUG drug type category.
LABELER NAME / MANUFACTURER: | Allergan, Inc. |
NON-PROPRIETARY NAME: | onabotulinumtoxinA |
SUBSTANCE NAME: | BOTULINUM TOXIN TYPE A |
TYPE: | HUMAN PRESCRIPTION DRUG |
PHARMA CLASS: | Acetylcholine Release Inhibitor [EPC],Acetylcholine Release Inhibitors [MoA] |
ROUTE: | INTRADERMAL; INTRAMUSCULAR |
DOSAGE FORM: | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
MARKETING CATEGORY NAME: | BLA |
START MARKETING DATE: | 1989-12-15 |
END MARKETING DATE: | 0000-00-00 |
BOTOX HUMAN PRESCRIPTION DRUG Details:
Item Description | BOTOX from Allergan, Inc. |
LABELER NAME: | Allergan, Inc. |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | 100([USP’U]/1) |
START MARKETING DATE: | 1989-12-15 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 0023-1145_e3d7b38d-cd47-4c2f-8808-e298499a7ba8 |
PRODUCT NDC: | 0023-1145 |
APPLICATION NUMBER: | BLA103000 |
Other BOTULINUM TOXIN TYPE A Pharmaceutical Manufacturers / Labelers: