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FDA Approval

Silver Sulfadiazine

FDA-approved pharmaceutical product with comprehensive regulatory information, manufacturing details, and complete labeling documentation.

FDA Approval Summary

Company
Effective Date
October 25, 2023
Labeling Type
HUMAN PRESCRIPTION DRUG LABEL
Silver sulfadiazine(10 mg in 1 g)

Manufacturing Establishments1

FDA-registered manufacturing facilities and establishments involved in the production, packaging, or distribution of this drug product.

A-S Medication Solutions

A-S Medication Solutions

830016429

Products1

Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.

Silver Sulfadiazine

Product Details

NDC Product Code
50090-0717
Application Number
NDA018810
Marketing Category
NDA (C73594)
Route of Administration
TOPICAL
Effective Date
December 6, 2017
Code: W46JY43EJRClass: ACTIBQuantity: 10 mg in 1 g
Stearyl AlcoholInactive
Code: 2KR89I4H1YClass: IACT
PetrolatumInactive
Code: 4T6H12BN9UClass: IACT
Polyoxyl 40 StearateInactive
Code: 13A4J4NH9IClass: IACT
Propylene GlycolInactive
Code: 6DC9Q167V3Class: IACT
Isopropyl MyristateInactive
Code: 0RE8K4LNJSClass: IACT
MethylparabenInactive
Code: A2I8C7HI9TClass: IACTQuantity: 3 mg in 1 g
Sorbitan MonooleateInactive
Code: 06XEA2VD56Class: IACT
WaterInactive
Code: 059QF0KO0RClass: IACT
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Silver Sulfadiazine - FDA Approval | MedPath