"52125-235-08" National Drug Code (NDC)

Albuterol Sulfate 10 TABLET in 1 BLISTER PACK (52125-235-08)
(REMEDYREPACK INC.)

NDC Code52125-235-08
Package Description10 TABLET in 1 BLISTER PACK (52125-235-08)
Product NDC52125-235
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameAlbuterol Sulfate
Non-Proprietary NameAlbuterol Sulfate
Dosage FormTABLET
UsageORAL
Start Marketing Date20130306
Marketing Category NameANDA
Application NumberANDA072637
ManufacturerREMEDYREPACK INC.
Substance NameALBUTEROL SULFATE
Strength2
Strength Unitmg/1
Pharmacy ClassesAdrenergic beta2-Agonists [MoA],beta2-Adrenergic Agonist [EPC]

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