Rosula - 10337-669-99 - (sodium sulfacetamide and sulfur)

Alphabetical Index


Drug Information of Rosula

Product NDC: 10337-669
Proprietary Name: Rosula
Non Proprietary Name: sodium sulfacetamide and sulfur
Active Ingredient(s): 100; 40    mg/g; mg/g & nbsp;   sodium sulfacetamide and sulfur
Administration Route(s): TOPICAL
Dosage Form(s): AEROSOL, FOAM
Coding System: National Drug Codes(NDC)

Labeler Information of Rosula

Product NDC: 10337-669
Labeler Name: PharmaDerm, A division of Nycomed US Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date: 20100803

Package Information of Rosula

Package NDC: 10337-669-99
Package Description: 1 CAN in 1 CARTON (10337-669-99) > 100 g in 1 CAN

NDC Information of Rosula

NDC Code 10337-669-99
Proprietary Name Rosula
Package Description 1 CAN in 1 CARTON (10337-669-99) > 100 g in 1 CAN
Product NDC 10337-669
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name sodium sulfacetamide and sulfur
Dosage Form Name AEROSOL, FOAM
Route Name TOPICAL
Start Marketing Date 20100803
Marketing Category Name UNAPPROVED DRUG OTHER
Labeler Name PharmaDerm, A division of Nycomed US Inc.
Substance Name SULFACETAMIDE SODIUM; SULFUR
Strength Number 100; 40
Strength Unit mg/g; mg/g
Pharmaceutical Classes Sulfonamide Antibacterial [EPC],Sulfonamides [Chemical/Ingredient]

Complete Information of Rosula


General Information