"70010-067-81" National Drug Code (NDC)

Ibuprofen 6 BLISTER PACK in 1 CARTON (70010-067-81) / 10 TABLET, FILM COATED in 1 BLISTER PACK
(Granules Pharmaceuticals Inc.)

NDC Code70010-067-81
Package Description6 BLISTER PACK in 1 CARTON (70010-067-81) / 10 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC70010-067
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameIbuprofen
Non-Proprietary NameIbuprofen
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20260218
Marketing Category NameANDA
Application NumberANDA091625
ManufacturerGranules Pharmaceuticals Inc.
Substance NameIBUPROFEN
Strength600
Strength Unitmg/1
Pharmacy ClassesAnti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Nonsteroidal Anti-inflammatory Drug [EPC]

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