"70518-1638-0" National Drug Code (NDC)

Pioglitazone Hydrochloride 90 TABLET in 1 BOTTLE, PLASTIC (70518-1638-0)
(REMEDYREPACK INC.)

NDC Code70518-1638-0
Package Description90 TABLET in 1 BOTTLE, PLASTIC (70518-1638-0)
Product NDC70518-1638
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NamePioglitazone Hydrochloride
Non-Proprietary NamePioglitazone Hydrochloride
Dosage FormTABLET
UsageORAL
Start Marketing Date20181106
End Marketing Date20251031
Marketing Category NameANDA
Application NumberANDA200044
ManufacturerREMEDYREPACK INC.
Substance NamePIOGLITAZONE HYDROCHLORIDE
Strength30
Strength Unitmg/1
Pharmacy ClassesPeroxisome Proliferator Receptor alpha Agonist [EPC], Peroxisome Proliferator Receptor gamma Agonist [EPC], Peroxisome Proliferator-activated Receptor alpha Agonists [MoA], Peroxisome Proliferator-activated Receptor gamma Agonists [MoA], Thiazolidinedione [EPC], Thiazolidinediones [CS]

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