"71205-898-90" National Drug Code (NDC)

Albuterol 90 TABLET in 1 BOTTLE (71205-898-90)
(Proficient Rx LP)

NDC Code71205-898-90
Package Description90 TABLET in 1 BOTTLE (71205-898-90)
Product NDC71205-898
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameAlbuterol
Non-Proprietary NameAlbuterol
Dosage FormTABLET
UsageORAL
Start Marketing Date20180629
Marketing Category NameANDA
Application NumberANDA207046
ManufacturerProficient Rx LP
Substance NameALBUTEROL SULFATE
Strength2
Strength Unitmg/1
Pharmacy ClassesAdrenergic beta2-Agonists [MoA], beta2-Adrenergic Agonist [EPC]

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