"61919-731-90" National Drug Code (NDC)

Pravastatin Sodium 90 TABLET in 1 BOTTLE (61919-731-90)
(DirectRX)

NDC Code61919-731-90
Package Description90 TABLET in 1 BOTTLE (61919-731-90)
Product NDC61919-731
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NamePravastatin Sodium
Non-Proprietary NamePravastatin Sodium
Dosage FormTABLET
UsageORAL
Start Marketing Date20151228
Marketing Category NameANDA
Application NumberANDA076939
ManufacturerDirectRX
Substance NamePRAVASTATIN SODIUM
Strength20
Strength Unitmg/1
Pharmacy ClassesHMG-CoA Reductase Inhibitor [EPC], Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]

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