Product NDC: | 43538-101 |
Proprietary Name: | Sumaxin CP |
Non Proprietary Name: | sulfacetamide sodium and sulfur |
Active Ingredient(s): | & nbsp; sulfacetamide sodium and sulfur |
Administration Route(s): | |
Dosage Form(s): | KIT |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 43538-101 |
Labeler Name: | Medimetriks Pharmaceuticals, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED DRUG OTHER |
Start Marketing Date: | 20110801 |
Package NDC: | 43538-101-60 |
Package Description: | 1 KIT in 1 CARTON (43538-101-60) * 60 PACKET in 1 CARTON > 3.7 g in 1 PACKET * 1 BOTTLE, PUMP in 1 CARTON > 454 g in 1 BOTTLE, PUMP |
NDC Code | 43538-101-60 |
Proprietary Name | Sumaxin CP |
Package Description | 1 KIT in 1 CARTON (43538-101-60) * 60 PACKET in 1 CARTON > 3.7 g in 1 PACKET * 1 BOTTLE, PUMP in 1 CARTON > 454 g in 1 BOTTLE, PUMP |
Product NDC | 43538-101 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | sulfacetamide sodium and sulfur |
Dosage Form Name | KIT |
Route Name | |
Start Marketing Date | 20110801 |
Marketing Category Name | UNAPPROVED DRUG OTHER |
Labeler Name | Medimetriks Pharmaceuticals, Inc. |
Substance Name | |
Strength Number | |
Strength Unit | |
Pharmaceutical Classes |