"69729-157-10" National Drug Code (NDC)

Ibuwin Forte 1 BLISTER PACK in 1 CARTON (69729-157-10) / 10 TABLET in 1 BLISTER PACK
(OPMX LLC)

NDC Code69729-157-10
Package Description1 BLISTER PACK in 1 CARTON (69729-157-10) / 10 TABLET in 1 BLISTER PACK
Product NDC69729-157
Product Type NameHUMAN OTC DRUG
Proprietary NameIbuwin Forte
Non-Proprietary NameIbuprofen
Dosage FormTABLET
UsageORAL
Start Marketing Date20231229
Marketing Category NameANDA
Application NumberANDA079174
ManufacturerOPMX LLC
Substance NameIBUPROFEN
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/69729-157-10