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"71205-899-30" National Drug Code (NDC)

Albuterol 30 TABLET in 1 BOTTLE (71205-899-30)
(Proficient Rx LP)

NDC Code71205-899-30
Package Description30 TABLET in 1 BOTTLE (71205-899-30)
Product NDC71205-899
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
Strength4
Strength Unitmg/1
Pharmacy ClassesAdrenergic beta2-Agonists [MoA], beta2-Adrenergic Agonist [EPC]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/71205-899-30





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