"72960-112-01" National Drug Code (NDC)

Daxxify 1 VIAL, SINGLE-USE in 1 CARTON (72960-112-01) / 1.2 mL in 1 VIAL, SINGLE-USE
(Revance Therapeutics, Inc.)

NDC Code72960-112-01
Package Description1 VIAL, SINGLE-USE in 1 CARTON (72960-112-01) / 1.2 mL in 1 VIAL, SINGLE-USE
Product NDC72960-112
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameDaxxify
Non-Proprietary NameBotulinum Toxin Type A
Dosage FormINJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
UsageINTRAMUSCULAR
Start Marketing Date20220920
Marketing Category NameBLA
Application NumberBLA761127
ManufacturerRevance Therapeutics, Inc.
Substance NameBOTULINUM TOXIN TYPE A
Strength100
Strength UnitU/1.2mL
Pharmacy ClassesAcetylcholine Release Inhibitor [EPC], Acetylcholine Release Inhibitors [MoA], Neuromuscular Blockade [PE], Neuromuscular Blocker [EPC]

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