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HYDROCORTISONE - 54505-331-05 - (hydrocortisone)

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Drug Information of HYDROCORTISONE

Product NDC: 54505-331
Proprietary Name: HYDROCORTISONE
Non Proprietary Name: hydrocortisone
Active Ingredient(s): 5    mg/1 & nbsp;   hydrocortisone
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of HYDROCORTISONE

Product NDC: 54505-331
Labeler Name: Lineage Therapeutics Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040646
Marketing Category: ANDA
Start Marketing Date: 20070330

Package Information of HYDROCORTISONE

Package NDC: 54505-331-05
Package Description: 50 TABLET in 1 BOTTLE, PLASTIC (54505-331-05)

NDC Information of HYDROCORTISONE

NDC Code 54505-331-05
Proprietary Name HYDROCORTISONE
Package Description 50 TABLET in 1 BOTTLE, PLASTIC (54505-331-05)
Product NDC 54505-331
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name hydrocortisone
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20070330
Marketing Category Name ANDA
Labeler Name Lineage Therapeutics Inc
Substance Name HYDROCORTISONE
Strength Number 5
Strength Unit mg/1
Pharmaceutical Classes Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]

Complete Information of HYDROCORTISONE


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