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Altabax
Altabax - 21695-644-10 - (retapamulin)
Drug Information of Altabax
| Product NDC: | 21695-644 |
| 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: | 21695-644 |
| Labeler Name: | Rebel Distributors Corp. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA022055 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20100107 |
Package Information of Altabax
| Package NDC: | 21695-644-10 |
| Package Description: | 10 g in 1 TUBE (21695-644-10) |
NDC Information of Altabax
| NDC Code | 21695-644-10 |
| Proprietary Name | Altabax |
| Package Description | 10 g in 1 TUBE (21695-644-10) |
| Product NDC | 21695-644 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | retapamulin |
| Dosage Form Name | OINTMENT |
| Route Name | TOPICAL |
| Start Marketing Date | 20100107 |
| Marketing Category Name | NDA |
| Labeler Name | Rebel Distributors Corp. |
| Substance Name | RETAPAMULIN |
| Strength Number | 10 |
| Strength Unit | mg/g |
| Pharmaceutical Classes | pleuromutilin [Chemical/Ingredient],Pleuromutilin Antibacterial [EPC] |
