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Hydrocortisone - 60429-262-01 - (Hydrocortisone)

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Drug Information of Hydrocortisone

Product NDC: 60429-262
Proprietary Name: Hydrocortisone
Non Proprietary Name: Hydrocortisone
Active Ingredient(s): 20    mg/1 & nbsp;   Hydrocortisone
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Hydrocortisone

Product NDC: 60429-262
Labeler Name: Golden State Medical Supply, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA083365
Marketing Category: ANDA
Start Marketing Date: 19730618

Package Information of Hydrocortisone

Package NDC: 60429-262-01
Package Description: 100 TABLET in 1 BOTTLE, PLASTIC (60429-262-01)

NDC Information of Hydrocortisone

NDC Code 60429-262-01
Proprietary Name Hydrocortisone
Package Description 100 TABLET in 1 BOTTLE, PLASTIC (60429-262-01)
Product NDC 60429-262
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Hydrocortisone
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19730618
Marketing Category Name ANDA
Labeler Name Golden State Medical Supply, Inc.
Substance Name HYDROCORTISONE
Strength Number 20
Strength Unit mg/1
Pharmaceutical Classes Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]

Complete Information of Hydrocortisone


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