Active Ingredient(s): Botulinum Toxin Type B
FDA Approved: * December 8, 2000
Pharm Company: * ELAN PHARM
Category: Neurological Disorders

* This drug may consist of multiple approval dates, manufacturers, or distributors. If applicable, they would be listed below under "NDC Database Records".

Myobloc Overview

Botulinum toxin (BoNT) is a neurotoxic protein produced by the bacterium Clostridium botulinum and related species.[1] It prevents the release of the neurotransmitter acetylcholine from axon endings at the neuromuscular junction, thus causing flaccid paralysis.[2] The toxin causes the disease botulism. The toxin is also used commercially for medical and cosmetic purposes. The seven main types of botulinum toxin are named types A to G (A, B, C1, C2, D, E, F and ...

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Possible Dosages for this and Related Drugs:

Botulinum Toxin Type B
  • Injection: 10000unit/2ml, 2500unit/0.5ml, 5000unit/ml
  • Vial: 5000iu/vial
Note: Above list includes dosages for all drugs with the same combination of active ingredients.

NDC Database Records for Myobloc: (3 results)

Sorted by National Drug Code
  • 10454-710 Myobloc 2500 [usp'u]/.5ml Intramuscular Injection, Solution by Solstice Neurosciences, LLC
  • 10454-711 Myobloc 5000 [usp'u]/Ml Intramuscular Injection, Solution by Solstice Neurosciences, LLC
  • 10454-712 Myobloc 10000 [usp'u]/2ml Intramuscular Injection, Solution by Solstice Neurosciences, LLC

Other drugs which contain Botulinum Toxin Type B or a similar ingredient: (1 result)