"53002-5700-3" National Drug Code (NDC)

Lovastatin 30 TABLET in 1 BOTTLE (53002-5700-3)
(RPK Pharmaceuticals, Inc.)

NDC Code53002-5700-3
Package Description30 TABLET in 1 BOTTLE (53002-5700-3)
Product NDC53002-5700
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameLovastatin
Non-Proprietary NameLovastatin
Dosage FormTABLET
UsageORAL
Start Marketing Date20071101
Marketing Category NameANDA
Application NumberANDA078296
ManufacturerRPK Pharmaceuticals, Inc.
Substance NameLOVASTATIN
Strength20
Strength Unitmg/1
Pharmacy ClassesHMG-CoA Reductase Inhibitor [EPC], Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]

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