SSD - 49884-600-36 - (silver sulfadiazine)

Alphabetical Index


Drug Information of SSD

Product NDC: 49884-600
Proprietary Name: SSD
Non Proprietary Name: silver sulfadiazine
Active Ingredient(s): 10    g/1000g & nbsp;   silver sulfadiazine
Administration Route(s): TOPICAL
Dosage Form(s): CREAM
Coding System: National Drug Codes(NDC)

Labeler Information of SSD

Product NDC: 49884-600
Labeler Name: Par Pharmaceutical Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA018578
Marketing Category: NDA
Start Marketing Date: 19970918

Package Information of SSD

Package NDC: 49884-600-36
Package Description: 50 g in 1 JAR (49884-600-36)

NDC Information of SSD

NDC Code 49884-600-36
Proprietary Name SSD
Package Description 50 g in 1 JAR (49884-600-36)
Product NDC 49884-600
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name silver sulfadiazine
Dosage Form Name CREAM
Route Name TOPICAL
Start Marketing Date 19970918
Marketing Category Name NDA
Labeler Name Par Pharmaceutical Inc.
Substance Name SILVER SULFADIAZINE
Strength Number 10
Strength Unit g/1000g
Pharmaceutical Classes Sulfonamide Antibacterial [EPC],Sulfonamides [Chemical/Ingredient]

Complete Information of SSD


General Information