ALTABAX - 0007-5180-22 - (retapamulin)

Alphabetical Index


Drug Information of ALTABAX

Product NDC: 0007-5180
Proprietary Name: ALTABAX
Non Proprietary Name: retapamulin
Active Ingredient(s): 10    mg/g & nbsp;   retapamulin
Administration Route(s): TOPICAL
Dosage Form(s): OINTMENT
Coding System: National Drug Codes(NDC)

Labeler Information of ALTABAX

Product NDC: 0007-5180
Labeler Name: GlaxoSmithKline LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA022055
Marketing Category: NDA
Start Marketing Date: 20070502

Package Information of ALTABAX

Package NDC: 0007-5180-22
Package Description: 15 g in 1 TUBE (0007-5180-22)

NDC Information of ALTABAX

NDC Code 0007-5180-22
Proprietary Name ALTABAX
Package Description 15 g in 1 TUBE (0007-5180-22)
Product NDC 0007-5180
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name retapamulin
Dosage Form Name OINTMENT
Route Name TOPICAL
Start Marketing Date 20070502
Marketing Category Name NDA
Labeler Name GlaxoSmithKline LLC
Substance Name RETAPAMULIN
Strength Number 10
Strength Unit mg/g
Pharmaceutical Classes pleuromutilin [Chemical/Ingredient],Pleuromutilin Antibacterial [EPC]

Complete Information of ALTABAX


General Information