Home > National Drug Code (NDC) > Dexamethasone

Dexamethasone - 63629-4129-2 - (Dexamethasone)

Alphabetical Index


Drug Information of Dexamethasone

Product NDC: 63629-4129
Proprietary Name: Dexamethasone
Non Proprietary Name: Dexamethasone
Active Ingredient(s): .75    mg/1 & nbsp;   Dexamethasone
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Dexamethasone

Product NDC: 63629-4129
Labeler Name: Bryant Ranch Prepack
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA084613
Marketing Category: ANDA
Start Marketing Date: 19750603

Package Information of Dexamethasone

Package NDC: 63629-4129-2
Package Description: 42 TABLET in 1 BOTTLE (63629-4129-2)

NDC Information of Dexamethasone

NDC Code 63629-4129-2
Proprietary Name Dexamethasone
Package Description 42 TABLET in 1 BOTTLE (63629-4129-2)
Product NDC 63629-4129
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Dexamethasone
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19750603
Marketing Category Name ANDA
Labeler Name Bryant Ranch Prepack
Substance Name DEXAMETHASONE
Strength Number .75
Strength Unit mg/1
Pharmaceutical Classes Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]

Complete Information of Dexamethasone


General Information