Home > National Drug Code (NDC) > Dexamethasone

Dexamethasone - 21695-745-12 - (Dexamethasone)

Alphabetical Index


Drug Information of Dexamethasone

Product NDC: 21695-745
Proprietary Name: Dexamethasone
Non Proprietary Name: Dexamethasone
Active Ingredient(s): 2    mg/1 & nbsp;   Dexamethasone
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Dexamethasone

Product NDC: 21695-745
Labeler Name: Rebel Distributors Corp
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA087916
Marketing Category: ANDA
Start Marketing Date: 19820826

Package Information of Dexamethasone

Package NDC: 21695-745-12
Package Description: 12 TABLET in 1 BOTTLE, PLASTIC (21695-745-12)

NDC Information of Dexamethasone

NDC Code 21695-745-12
Proprietary Name Dexamethasone
Package Description 12 TABLET in 1 BOTTLE, PLASTIC (21695-745-12)
Product NDC 21695-745
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Dexamethasone
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19820826
Marketing Category Name ANDA
Labeler Name Rebel Distributors Corp
Substance Name DEXAMETHASONE
Strength Number 2
Strength Unit mg/1
Pharmaceutical Classes Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]

Complete Information of Dexamethasone


General Information