"59651-333-05" National Drug Code (NDC)

Albuterol 500 TABLET in 1 BOTTLE (59651-333-05)
(Aurobindo Pharma Limited)

NDC Code59651-333-05
Package Description500 TABLET in 1 BOTTLE (59651-333-05)
Product NDC59651-333
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameAlbuterol
Non-Proprietary NameAlbuterol
Dosage FormTABLET
UsageORAL
Start Marketing Date20200514
Marketing Category NameANDA
Application NumberANDA213657
ManufacturerAurobindo Pharma Limited
Substance NameALBUTEROL SULFATE
Strength2
Strength Unitmg/1
Pharmacy ClassesAdrenergic beta2-Agonists [MoA], beta2-Adrenergic Agonist [EPC]

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