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"0093-7201-10" National Drug Code (NDC)

Pravastatin Sodium 1000 TABLET in 1 BOTTLE (0093-7201-10)
(Teva Pharmaceuticals USA, Inc.)

NDC Code0093-7201-10
Package Description1000 TABLET in 1 BOTTLE (0093-7201-10)
Product NDC0093-7201
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NamePravastatin Sodium
Non-Proprietary NamePravastatin Sodium
Dosage FormTABLET
UsageORAL
Start Marketing Date20060425
Marketing Category NameANDA
Application NumberANDA076056
ManufacturerTeva Pharmaceuticals USA, Inc.
Substance NamePRAVASTATIN SODIUM
Strength20
Strength Unitmg/1
Pharmacy ClassesHMG-CoA Reductase Inhibitor [EPC], Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/0093-7201-10





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