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Dexamethasone - 52959-547-21 - (dexamethasone)

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Drug Information of Dexamethasone

Product NDC: 52959-547
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: 52959-547
Labeler Name: H.J. Harkins Company, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA088238
Marketing Category: ANDA
Start Marketing Date: 19830428

Package Information of Dexamethasone

Package NDC: 52959-547-21
Package Description: 21 TABLET in 1 BOTTLE, PLASTIC (52959-547-21)

NDC Information of Dexamethasone

NDC Code 52959-547-21
Proprietary Name Dexamethasone
Package Description 21 TABLET in 1 BOTTLE, PLASTIC (52959-547-21)
Product NDC 52959-547
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name dexamethasone
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19830428
Marketing Category Name ANDA
Labeler Name H.J. Harkins Company, Inc.
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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