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Dexamethasone - 21695-382-20 - (Dexamethasone)

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Drug Information of Dexamethasone

Product NDC: 21695-382
Proprietary Name: Dexamethasone
Non Proprietary Name: Dexamethasone
Active Ingredient(s): 4    mg/1 & nbsp;   Dexamethasone
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Dexamethasone

Product NDC: 21695-382
Labeler Name: Rebel Distributors Corp
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA084612
Marketing Category: ANDA
Start Marketing Date: 19780719

Package Information of Dexamethasone

Package NDC: 21695-382-20
Package Description: 20 TABLET in 1 BOTTLE, PLASTIC (21695-382-20)

NDC Information of Dexamethasone

NDC Code 21695-382-20
Proprietary Name Dexamethasone
Package Description 20 TABLET in 1 BOTTLE, PLASTIC (21695-382-20)
Product NDC 21695-382
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Dexamethasone
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19780719
Marketing Category Name ANDA
Labeler Name Rebel Distributors Corp
Substance Name DEXAMETHASONE
Strength Number 4
Strength Unit mg/1
Pharmaceutical Classes Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]

Complete Information of Dexamethasone


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