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"70771-1512-5" National Drug Code (NDC)

Albuterol 500 TABLET in 1 BOTTLE (70771-1512-5)
(Zydus Lifesciences Limited)

NDC Code70771-1512-5
Package Description500 TABLET in 1 BOTTLE (70771-1512-5)
Product NDC70771-1512
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameAlbuterol
Non-Proprietary NameAlbuterol
Dosage FormTABLET
UsageORAL
Start Marketing Date20201023
Marketing Category NameANDA
Application NumberANDA208884
ManufacturerZydus Lifesciences Limited
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/70771-1512-5





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