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Hydrocortisone Acetate - 0574-7090-12 - (HYDROCORTISONE ACETATE)

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Drug Information of Hydrocortisone Acetate

Product NDC: 0574-7090
Proprietary Name: Hydrocortisone Acetate
Non Proprietary Name: HYDROCORTISONE ACETATE
Active Ingredient(s): 25    mg/1 & nbsp;   HYDROCORTISONE ACETATE
Administration Route(s): RECTAL
Dosage Form(s): SUPPOSITORY
Coding System: National Drug Codes(NDC)

Labeler Information of Hydrocortisone Acetate

Product NDC: 0574-7090
Labeler Name: Paddock Laboratories, LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date: 19900701

Package Information of Hydrocortisone Acetate

Package NDC: 0574-7090-12
Package Description: 12 PACKET in 1 BOX (0574-7090-12) > 1 SUPPOSITORY in 1 PACKET

NDC Information of Hydrocortisone Acetate

NDC Code 0574-7090-12
Proprietary Name Hydrocortisone Acetate
Package Description 12 PACKET in 1 BOX (0574-7090-12) > 1 SUPPOSITORY in 1 PACKET
Product NDC 0574-7090
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name HYDROCORTISONE ACETATE
Dosage Form Name SUPPOSITORY
Route Name RECTAL
Start Marketing Date 19900701
Marketing Category Name UNAPPROVED DRUG OTHER
Labeler Name Paddock Laboratories, LLC
Substance Name HYDROCORTISONE ACETATE
Strength Number 25
Strength Unit mg/1
Pharmaceutical Classes Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]

Complete Information of Hydrocortisone Acetate


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