"0093-7152-31" National Drug Code (NDC)

Simvastatin 1 BLISTER PACK in 1 CARTON (0093-7152-31) > 30 TABLET, FILM COATED in 1 BLISTER PACK
(Teva Pharmaceuticals USA, Inc.)

NDC Code0093-7152-31
Package Description1 BLISTER PACK in 1 CARTON (0093-7152-31) > 30 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC0093-7152
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameSimvastatin
Non-Proprietary NameSimvastatin
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20060627
Marketing Category NameANDA
Application NumberANDA076052
ManufacturerTeva Pharmaceuticals USA, Inc.
Substance NameSIMVASTATIN
Strength5
Strength Unitmg/1
Pharmacy ClassesHMG-CoA Reductase Inhibitor [EPC],Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]

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