"70512-780-50" National Drug Code (NDC)

Ibuprofen 500 TABLET in 1 BOTTLE (70512-780-50)
(SOLA Pharmaceuticals, LLC)

NDC Code70512-780-50
Package Description500 TABLET in 1 BOTTLE (70512-780-50)
Product NDC70512-780
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameIbuprofen
Non-Proprietary NameIbuprofen
Dosage FormTABLET
UsageORAL
Start Marketing Date20241201
Marketing Category NameANDA
Application NumberANDA078329
ManufacturerSOLA Pharmaceuticals, LLC
Substance NameIBUPROFEN
Strength800
Strength Unitmg/1
Pharmacy ClassesAnti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Nonsteroidal Anti-inflammatory Drug [EPC]

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