59762-0074 NDC - HYDROCORTISONE (HYDROCORTISONE)

Drug Information

Product NDC: 59762-0074

Proprietary Name: Hydrocortisone

Non Proprietary Name: hydrocortisone

Active Ingredient(s):
  • 10 mg/1 HYDROCORTISONE


Administration Route(s): ORAL

Dosage Form(s): TABLET

Pharmacy Class(es):
  • Corticosteroid [EPC];
  • Corticosteroid Hormone Receptor Agonists [MoA]

Labeler Information

Labeler Name: Greenstone LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA008697
Marketing Category: NDA AUTHORIZED GENERIC
Start Marketing Date:2/20/2013

Package Information

No. Package Code Package Description
1 59762-0074-1 100 TABLET in 1 BOTTLE (59762-0074-1)

NDC Record

No. Field Name Field Value
1 PRODUCT NDC 59762-0074
2 PRODUCT TYPE NAME HUMAN PRESCRIPTION DRUG
3 PROPRIETARY NAME Hydrocortisone
4 NON PROPRIETARY NAME hydrocortisone
5 DOSAGE FORM NAME TABLET
6 ROUTE NAME ORAL
7 START MARKETING DATE 2/20/2013
8 MARKETING CATEGORY NAME NDA AUTHORIZED GENERIC
9 APPLICATION NUMBER NDA008697
10 LABELER NAME Greenstone LLC
11 SUBSTANCE NAME HYDROCORTISONE
12 ACTIVE NUMERATOR STRENGTH 10
13 ACTIVE INGRED UNIT mg/1
14 PHARM CLASSES Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]

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This page was last updated on: 7/25/2014