Details for New Drug Application (NDA): 011664
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NDA 011664 describes DECADRON, which is a drug marketed by Merck and is included in eight NDAs. Additional details are available on the DECADRON profile page.
The generic ingredient in DECADRON is dexamethasone acetate. There are four drug master file entries for this compound. Additional details are available on the dexamethasone acetate profile page.
The generic ingredient in DECADRON is dexamethasone acetate. There are four drug master file entries for this compound. Additional details are available on the dexamethasone acetate profile page.
Summary for 011664
| Tradename: | DECADRON |
| Applicant: | Merck |
| Ingredient: | dexamethasone |
| Patents: | 0 |
Medical Subject Heading (MeSH) Categories for 011664
Profile for product number 001
| Active Rx/OTC/Discontinued: | DISCN | Dosage: | TABLET;ORAL | Strength | 0.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | ||||
| Approval Date: | Approved Prior to Jan 1, 1982 | TE: | RLD: | Yes | |||||
Profile for product number 002
| Active Rx/OTC/Discontinued: | DISCN | Dosage: | TABLET;ORAL | Strength | 0.75MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | ||||
| Approval Date: | Approved Prior to Jan 1, 1982 | TE: | RLD: | Yes | |||||
Profile for product number 003
| Active Rx/OTC/Discontinued: | DISCN | Dosage: | TABLET;ORAL | Strength | 1.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | ||||
| Approval Date: | Approved Prior to Jan 1, 1982 | TE: | RLD: | Yes | |||||
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