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"61919-621-30" National Drug Code (NDC)

Ibu 30 TABLET in 1 BOTTLE (61919-621-30)
(DirectRX)

NDC Code61919-621-30
Package Description30 TABLET in 1 BOTTLE (61919-621-30)
Product NDC61919-621
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameIbu
Non-Proprietary NameIbu
Dosage FormTABLET
UsageORAL
Start Marketing Date20190430
Marketing Category NameANDA
Application NumberANDA075682
ManufacturerDirectRX
Substance NameIBUPROFEN
Strength800
Strength Unitmg/1
Pharmacy ClassesCyclooxygenase Inhibitors [MoA],Anti-Inflammatory Agents, Non-Steroidal [CS],Nonsteroidal Anti-inflammatory Drug [EPC]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/61919-621-30





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