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"70710-1062-5" National Drug Code (NDC)

Albuterol 500 TABLET in 1 BOTTLE (70710-1062-5)
(Zydus Pharmaceuticals USA Inc.)

NDC Code70710-1062-5
Package Description500 TABLET in 1 BOTTLE (70710-1062-5)
Product NDC70710-1062
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameAlbuterol
Non-Proprietary NameAlbuterol
Dosage FormTABLET
UsageORAL
Start Marketing Date20201023
Marketing Category NameANDA
Application NumberANDA208884
ManufacturerZydus Pharmaceuticals USA Inc.
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/70710-1062-5





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