"68001-200-03" National Drug Code (NDC)

Diclofenac Sodium 500 TABLET, DELAYED RELEASE in 1 BOTTLE (68001-200-03)
(BluePoint Laboratories)

NDC Code68001-200-03
Package Description500 TABLET, DELAYED RELEASE in 1 BOTTLE (68001-200-03)
Product NDC68001-200
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameDiclofenac Sodium
Non-Proprietary NameDiclofenac Sodium
Dosage FormTABLET, DELAYED RELEASE
UsageORAL
Start Marketing Date20140224
Marketing Category NameANDA
Application NumberANDA074394
ManufacturerBluePoint Laboratories
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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