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"0007-5180-22" National Drug Code (NDC)

Altabax 1 TUBE in 1 CARTON (0007-5180-22) > 15 g in 1 TUBE
(GlaxoSmithKline LLC)

NDC Code0007-5180-22
Package Description1 TUBE in 1 CARTON (0007-5180-22) > 15 g in 1 TUBE
Product NDC0007-5180
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameAltabax
Non-Proprietary NameRetapamulin
Dosage FormOINTMENT
UsageTOPICAL
Start Marketing Date20070502
End Marketing Date20170101
Marketing Category NameNDA
Application NumberNDA022055
ManufacturerGlaxoSmithKline LLC
Substance NameRETAPAMULIN
Strength10
Strength Unitmg/g
Pharmacy Classespleuromutilin [Chemical/Ingredient],Pleuromutilin Antibacterial [EPC]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/0007-5180-22





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