"68071-3132-1" National Drug Code (NDC)

Diclofenac Sodium 120 TABLET, DELAYED RELEASE in 1 BOTTLE (68071-3132-1)
(NuCare Pharmaceuticals, Inc.)

NDC Code68071-3132-1
Package Description120 TABLET, DELAYED RELEASE in 1 BOTTLE (68071-3132-1)
Product NDC68071-3132
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameDiclofenac Sodium
Non-Proprietary NameDiclofenac Sodium
Dosage FormTABLET, DELAYED RELEASE
UsageORAL
Start Marketing Date19951130
Marketing Category NameANDA
Application NumberANDA074394
ManufacturerNuCare Pharmaceuticals, Inc.
Substance NameDICLOFENAC SODIUM
Strength75
Strength Unitmg/1
Pharmacy ClassesCyclooxygenase Inhibitors [MoA],Decreased Prostaglandin Production [PE],Anti-Inflammatory Agents, Non-Steroidal [CS],Nonsteroidal Anti-inflammatory Drug [EPC]

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