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Hydrocortisone - 0603-7785-52 - (hydrocortisone)

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Drug Information of Hydrocortisone

Product NDC: 0603-7785
Proprietary Name: Hydrocortisone
Non Proprietary Name: hydrocortisone
Active Ingredient(s): 25    mg/mL & nbsp;   hydrocortisone
Administration Route(s): TOPICAL
Dosage Form(s): LOTION
Coding System: National Drug Codes(NDC)

Labeler Information of Hydrocortisone

Product NDC: 0603-7785
Labeler Name: Qualitest Pharmaceuticals
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040417
Marketing Category: ANDA
Start Marketing Date: 20030730

Package Information of Hydrocortisone

Package NDC: 0603-7785-52
Package Description: 1 BOTTLE, PLASTIC in 1 CARTON (0603-7785-52) > 59 mL in 1 BOTTLE, PLASTIC

NDC Information of Hydrocortisone

NDC Code 0603-7785-52
Proprietary Name Hydrocortisone
Package Description 1 BOTTLE, PLASTIC in 1 CARTON (0603-7785-52) > 59 mL in 1 BOTTLE, PLASTIC
Product NDC 0603-7785
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name hydrocortisone
Dosage Form Name LOTION
Route Name TOPICAL
Start Marketing Date 20030730
Marketing Category Name ANDA
Labeler Name Qualitest Pharmaceuticals
Substance Name HYDROCORTISONE
Strength Number 25
Strength Unit mg/mL
Pharmaceutical Classes Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]

Complete Information of Hydrocortisone


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