"0023-3921-02" National Drug Code (NDC)

Botox 1 VIAL in 1 CARTON (0023-3921-02) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL
(Allergan, Inc.)

NDC Code0023-3921-02
Package Description1 VIAL in 1 CARTON (0023-3921-02) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL
Product NDC0023-3921
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameBotox
Non-Proprietary NameOnabotulinumtoxina
Dosage FormINJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
UsageINTRADERMAL; INTRAMUSCULAR
Start Marketing Date20100111
Marketing Category NameBLA
Application NumberBLA103000
ManufacturerAllergan, Inc.
Substance NameBOTULINUM TOXIN TYPE A
Strength200
Strength Unit[USP'U]/1
Pharmacy ClassesAcetylcholine Release Inhibitor [EPC], Acetylcholine Release Inhibitors [MoA], Neuromuscular Blockade [PE], Neuromuscular Blocker [EPC]

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