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A-HYDROCORT - 0409-4856-05 - (HYDROCORTISONE SODIUM SUCCINATE)

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Drug Information of A-HYDROCORT

Product NDC: 0409-4856
Proprietary Name: A-HYDROCORT
Non Proprietary Name: HYDROCORTISONE SODIUM SUCCINATE
Active Ingredient(s): 100    mg/2mL & nbsp;   HYDROCORTISONE SODIUM SUCCINATE
Administration Route(s): INTRAMUSCULAR; INTRAVENOUS
Dosage Form(s): INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of A-HYDROCORT

Product NDC: 0409-4856
Labeler Name: Hospira, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040666
Marketing Category: ANDA
Start Marketing Date: 20110512

Package Information of A-HYDROCORT

Package NDC: 0409-4856-05
Package Description: 10 VIAL, SINGLE-DOSE in 1 CARTON (0409-4856-05) > 2 mL in 1 VIAL, SINGLE-DOSE

NDC Information of A-HYDROCORT

NDC Code 0409-4856-05
Proprietary Name A-HYDROCORT
Package Description 10 VIAL, SINGLE-DOSE in 1 CARTON (0409-4856-05) > 2 mL in 1 VIAL, SINGLE-DOSE
Product NDC 0409-4856
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name HYDROCORTISONE SODIUM SUCCINATE
Dosage Form Name INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Route Name INTRAMUSCULAR; INTRAVENOUS
Start Marketing Date 20110512
Marketing Category Name ANDA
Labeler Name Hospira, Inc.
Substance Name HYDROCORTISONE SODIUM SUCCINATE
Strength Number 100
Strength Unit mg/2mL
Pharmaceutical Classes Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]

Complete Information of A-HYDROCORT


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