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Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

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Product Details for NDA 011664

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DECADRON (DEXAMETHASONE)
0.25MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Marketing Status: Discontinued
Active Ingredient: DEXAMETHASONE
Proprietary Name: DECADRON
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 0.25MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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: N011664
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
DECADRON (DEXAMETHASONE)
0.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Marketing Status: Discontinued
Active Ingredient: DEXAMETHASONE
Proprietary Name: DECADRON
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 0.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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: N011664
Product Number: 001
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)
0.75MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Marketing Status: Discontinued
Active Ingredient: DEXAMETHASONE
Proprietary Name: DECADRON
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 0.75MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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: N011664
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)
1.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Marketing Status: Discontinued
Active Ingredient: DEXAMETHASONE
Proprietary Name: DECADRON
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 1.5MG **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: N011664
Product Number: 003
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)
4MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Marketing Status: Discontinued
Active Ingredient: DEXAMETHASONE
Proprietary Name: DECADRON
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 4MG **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: N011664
Product Number: 005
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)
6MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Marketing Status: Discontinued
Active Ingredient: DEXAMETHASONE
Proprietary Name: DECADRON
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 6MG **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: N011664
Product Number: 006
Approval Date: Jul 30, 1982
Applicant Holder Full Name: MERCK AND CO INC
Marketing Status:  Discontinued
Patent and Exclusivity Information
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