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"61919-211-30" National Drug Code (NDC)

Sunlindac 30 TABLET in 1 BOTTLE (61919-211-30)
(Direct Rx)

NDC Code61919-211-30
Package Description30 TABLET in 1 BOTTLE (61919-211-30)
Product NDC61919-211
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameSunlindac
Non-Proprietary NameSulindac
Dosage FormTABLET
UsageORAL
Start Marketing Date20140101
Marketing Category NameANDA
Application NumberANDA072051
ManufacturerDirect Rx
Substance NameSULINDAC
Strength200
Strength Unitmg/1
Pharmacy ClassesAnti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Nonsteroidal Anti-inflammatory Drug [EPC]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/61919-211-30





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