SE 10-5 SS - 13925-114-04 - (SODIUM SULFACETAMIDE, SULFUR)

Alphabetical Index


Drug Information of SE 10-5 SS

Product NDC: 13925-114
Proprietary Name: SE 10-5 SS
Non Proprietary Name: SODIUM SULFACETAMIDE, SULFUR
Active Ingredient(s): 100; 50    mg/g; mg/g & nbsp;   SODIUM SULFACETAMIDE, SULFUR
Administration Route(s): TOPICAL
Dosage Form(s): CREAM
Coding System: National Drug Codes(NDC)

Labeler Information of SE 10-5 SS

Product NDC: 13925-114
Labeler Name: Seton Pharmaceuticals
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date: 20100515

Package Information of SE 10-5 SS

Package NDC: 13925-114-04
Package Description: 1 TUBE in 1 CARTON (13925-114-04) > 113.4 g in 1 TUBE

NDC Information of SE 10-5 SS

NDC Code 13925-114-04
Proprietary Name SE 10-5 SS
Package Description 1 TUBE in 1 CARTON (13925-114-04) > 113.4 g in 1 TUBE
Product NDC 13925-114
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name SODIUM SULFACETAMIDE, SULFUR
Dosage Form Name CREAM
Route Name TOPICAL
Start Marketing Date 20100515
Marketing Category Name UNAPPROVED DRUG OTHER
Labeler Name Seton Pharmaceuticals
Substance Name SULFACETAMIDE SODIUM; SULFUR
Strength Number 100; 50
Strength Unit mg/g; mg/g
Pharmaceutical Classes Sulfonamide Antibacterial [EPC],Sulfonamides [Chemical/Ingredient]

Complete Information of SE 10-5 SS


General Information