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"48792-7811-1" National Drug Code (NDC)

Ibuprofen 50 TABLET, FILM COATED in 1 BOTTLE (48792-7811-1)
(Sunshine Lake Pharma Co., Ltd.)

NDC Code48792-7811-1
Package Description50 TABLET, FILM COATED in 1 BOTTLE (48792-7811-1)
Product NDC48792-7811
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameIbuprofen
Non-Proprietary NameIbuprofen
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20180910
Marketing Category NameANDA
Application NumberANDA204062
ManufacturerSunshine Lake Pharma Co., Ltd.
Substance NameIBUPROFEN
Strength800
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/48792-7811-1





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