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"31722-752-31" National Drug Code (NDC)

Lamivudine 10 TABLET, FILM COATED in 1 BLISTER PACK (31722-752-31)
(Camber Pharmaceuticals, Inc.)

NDC Code31722-752-31
Package Description10 TABLET, FILM COATED in 1 BLISTER PACK (31722-752-31)
Product NDC31722-752
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameLamivudine
Non-Proprietary NameLamivudine
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20140102
Marketing Category NameANDA
Application NumberANDA203260
ManufacturerCamber Pharmaceuticals, Inc.
Substance NameLAMIVUDINE
Strength100
Strength Unitmg/1
Pharmacy ClassesHepatitis B Virus Nucleoside Analog Reverse Transcriptase Inhibitor [EPC], Human Immunodeficiency Virus Nucleoside Analog Reverse Transcriptase Inhibitor [EPC], Nucleoside Analog [EXT], Nucleoside Reverse Transcriptase Inhibitors [MoA]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/31722-752-31





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