"65841-739-05" National Drug Code (NDC)

Pravastatin Sodium 500 TABLET in 1 BOTTLE (65841-739-05)
(Zydus Lifesciences Limited)

NDC Code65841-739-05
Package Description500 TABLET in 1 BOTTLE (65841-739-05)
Product NDC65841-739
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NamePravastatin Sodium
Non-Proprietary NamePravastatin Sodium
Dosage FormTABLET
UsageORAL
Start Marketing Date20100330
Marketing Category NameANDA
Application NumberANDA077751
ManufacturerZydus Lifesciences Limited
Substance NamePRAVASTATIN SODIUM
Strength10
Strength Unitmg/1
Pharmacy ClassesHMG-CoA Reductase Inhibitor [EPC], Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]

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