CORTEF - 0009-0031-01 - (hydrocortisone)

Alphabetical Index


Drug Information of CORTEF

Product NDC: 0009-0031
Proprietary Name: CORTEF
Non Proprietary Name: hydrocortisone
Active Ingredient(s): 10    mg/1 & nbsp;   hydrocortisone
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of CORTEF

Product NDC: 0009-0031
Labeler Name: Pharmacia and Upjohn Company
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA008697
Marketing Category: NDA
Start Marketing Date: 19521215

Package Information of CORTEF

Package NDC: 0009-0031-01
Package Description: 100 TABLET in 1 BOTTLE (0009-0031-01)

NDC Information of CORTEF

NDC Code 0009-0031-01
Proprietary Name CORTEF
Package Description 100 TABLET in 1 BOTTLE (0009-0031-01)
Product NDC 0009-0031
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name hydrocortisone
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19521215
Marketing Category Name NDA
Labeler Name Pharmacia and Upjohn Company
Substance Name HYDROCORTISONE
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]

Complete Information of CORTEF


General Information