Product Details for NDA 012071
DECADRON (DEXAMETHASONE SODIUM PHOSPHATE)
EQ 4MG PHOSPHATE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Marketing Status: Discontinued
EQ 24MG PHOSPHATE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Marketing Status: Discontinued
EQ 4MG PHOSPHATE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Marketing Status: Discontinued
Active Ingredient: DEXAMETHASONE SODIUM PHOSPHATE
Proprietary Name: DECADRON
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: EQ 4MG PHOSPHATE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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: N012071
Product Number: 002
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: MERCK AND CO INC
Marketing Status: Discontinued
Patent and Exclusivity Information
DECADRON (DEXAMETHASONE SODIUM PHOSPHATE)
Proprietary Name: DECADRON
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: EQ 4MG PHOSPHATE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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: N012071
Product Number: 002
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: MERCK AND CO INC
Marketing Status: Discontinued
Patent and Exclusivity Information
EQ 24MG PHOSPHATE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Marketing Status: Discontinued
Active Ingredient: DEXAMETHASONE SODIUM PHOSPHATE
Proprietary Name: DECADRON
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: EQ 24MG PHOSPHATE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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: N012071
Product Number: 004
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: MERCK AND CO INC
Marketing Status: Discontinued
Patent and Exclusivity Information
Proprietary Name: DECADRON
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: EQ 24MG PHOSPHATE/ML **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: N012071
Product Number: 004
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: MERCK AND CO INC
Marketing Status: Discontinued
Patent and Exclusivity Information