"48792-7813-1" National Drug Code (NDC)

Ibuprofen 100 TABLET, FILM COATED in 1 BOTTLE (48792-7813-1)
(Sunshine Lake Pharma Co., Ltd.)

NDC Code48792-7813-1
Package Description100 TABLET, FILM COATED in 1 BOTTLE (48792-7813-1)
Product NDC48792-7813
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameIbuprofen
Non-Proprietary NameIbuprofen
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20180924
Marketing Category NameANDA
Application NumberANDA204062
ManufacturerSunshine Lake Pharma Co., Ltd.
Substance NameIBUPROFEN
Strength400
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/48792-7813-1