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"48792-7865-1" National Drug Code (NDC)

Linagliptin 30 TABLET, FILM COATED in 1 BOTTLE (48792-7865-1)
(Sunshine Lake Pharma Co., Ltd.)

NDC Code48792-7865-1
Package Description30 TABLET, FILM COATED in 1 BOTTLE (48792-7865-1)
Product NDC48792-7865
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameLinagliptin
Non-Proprietary NameLinagliptin
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20260101
Marketing Category NameANDA
Application NumberANDA208335
ManufacturerSunshine Lake Pharma Co., Ltd.
Substance NameLINAGLIPTIN
Strength5
Strength Unitmg/1
Pharmacy ClassesDipeptidyl Peptidase 4 Inhibitor [EPC], Dipeptidyl Peptidase 4 Inhibitors [MoA]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/48792-7865-1





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