Product Details for NDA 005963
SODIUM SULAMYD (SULFACETAMIDE SODIUM)
10% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Marketing Status: Discontinued
10% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Marketing Status: Discontinued
30% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Marketing Status: Discontinued
10% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Marketing Status: Discontinued
Active Ingredient: SULFACETAMIDE SODIUM
Proprietary Name: SODIUM SULAMYD
Dosage Form; Route of Administration: OINTMENT; OPHTHALMIC
Strength: 10% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Reference Listed Drug: Yes
Reference Standard: No
TE Code:
Application Number: N005963
Product Number: 002
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: SCHERING CORP SUB SCHERING PLOUGH CORP
Marketing Status: Discontinued
Patent and Exclusivity Information
SODIUM SULAMYD (SULFACETAMIDE SODIUM)
Proprietary Name: SODIUM SULAMYD
Dosage Form; Route of Administration: OINTMENT; OPHTHALMIC
Strength: 10% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Reference Listed Drug: Yes
Reference Standard: No
TE Code:
Application Number: N005963
Product Number: 002
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: SCHERING CORP SUB SCHERING PLOUGH CORP
Marketing Status: Discontinued
Patent and Exclusivity Information
10% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Marketing Status: Discontinued
Active Ingredient: SULFACETAMIDE SODIUM
Proprietary Name: SODIUM SULAMYD
Dosage Form; Route of Administration: SOLUTION/DROPS; OPHTHALMIC
Strength: 10% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Reference Listed Drug: Yes
Reference Standard: No
TE Code:
Application Number: N005963
Product Number: 001
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: SCHERING CORP SUB SCHERING PLOUGH CORP
Marketing Status: Discontinued
Patent and Exclusivity Information
SODIUM SULAMYD (SULFACETAMIDE SODIUM)
Proprietary Name: SODIUM SULAMYD
Dosage Form; Route of Administration: SOLUTION/DROPS; OPHTHALMIC
Strength: 10% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Reference Listed Drug: Yes
Reference Standard: No
TE Code:
Application Number: N005963
Product Number: 001
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: SCHERING CORP SUB SCHERING PLOUGH CORP
Marketing Status: Discontinued
Patent and Exclusivity Information
30% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Marketing Status: Discontinued
Active Ingredient: SULFACETAMIDE SODIUM
Proprietary Name: SODIUM SULAMYD
Dosage Form; Route of Administration: SOLUTION/DROPS; OPHTHALMIC
Strength: 30% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Reference Listed Drug: Yes
Reference Standard: No
TE Code:
Application Number: N005963
Product Number: 003
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: SCHERING CORP SUB SCHERING PLOUGH CORP
Marketing Status: Discontinued
Patent and Exclusivity Information
Proprietary Name: SODIUM SULAMYD
Dosage Form; Route of Administration: SOLUTION/DROPS; OPHTHALMIC
Strength: 30% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Reference Listed Drug: Yes
Reference Standard: No
TE Code:
Application Number: N005963
Product Number: 003
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: SCHERING CORP SUB SCHERING PLOUGH CORP
Marketing Status: Discontinued
Patent and Exclusivity Information