"0173-0736-01" National Drug Code (NDC)

Imitrex 1 CARTON in 1 CARTON (0173-0736-01) / 1 BLISTER PACK in 1 CARTON / 9 TABLET, FILM COATED in 1 BLISTER PACK
(GlaxoSmithKline LLC)

NDC Code0173-0736-01
Package Description1 CARTON in 1 CARTON (0173-0736-01) / 1 BLISTER PACK in 1 CARTON / 9 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC0173-0736
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameImitrex
Non-Proprietary NameSumatriptan
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20031217
Marketing Category NameNDA
Application NumberNDA020132
ManufacturerGlaxoSmithKline LLC
Substance NameSUMATRIPTAN SUCCINATE
Strength50
Strength Unitmg/1
Pharmacy ClassesSerotonin 1b Receptor Agonists [MoA], Serotonin 1d Receptor Agonists [MoA], Serotonin-1b and Serotonin-1d Receptor Agonist [EPC]

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