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Hydrocortisone - 49999-139-01 - (Hydrocortisone)

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Drug Information of Hydrocortisone

Product NDC: 49999-139
Proprietary Name: Hydrocortisone
Non Proprietary Name: Hydrocortisone
Active Ingredient(s): 10    mg/g & nbsp;   Hydrocortisone
Administration Route(s): TOPICAL
Dosage Form(s): CREAM
Coding System: National Drug Codes(NDC)

Labeler Information of Hydrocortisone

Product NDC: 49999-139
Labeler Name: Lake Erie Medical DBA Quality Care Products LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA080693
Marketing Category: ANDA
Start Marketing Date: 19760430

Package Information of Hydrocortisone

Package NDC: 49999-139-01
Package Description: 28.35 g in 1 TUBE (49999-139-01)

NDC Information of Hydrocortisone

NDC Code 49999-139-01
Proprietary Name Hydrocortisone
Package Description 28.35 g in 1 TUBE (49999-139-01)
Product NDC 49999-139
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Hydrocortisone
Dosage Form Name CREAM
Route Name TOPICAL
Start Marketing Date 19760430
Marketing Category Name ANDA
Labeler Name Lake Erie Medical DBA Quality Care Products LLC
Substance Name HYDROCORTISONE
Strength Number 10
Strength Unit mg/g
Pharmaceutical Classes Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]

Complete Information of Hydrocortisone


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