cortef

Generic: hydrocortisone

Labeler: pharmacia & upjohn company llc
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name cortef
Generic Name hydrocortisone
Labeler pharmacia & upjohn company llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

hydrocortisone 20 mg/1

Manufacturer
Pharmacia & Upjohn Company LLC

Identifiers & Regulatory

Product NDC 0009-0044
Product ID 0009-0044_17306ca2-c631-4281-824c-1cb6d63dcac1
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA008697
Listing Expiration 2026-12-31
Marketing Start 1952-12-15

Pharmacologic Class

Established (EPC)
corticosteroid [epc]
Mechanism of Action
corticosteroid hormone receptor agonists [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 00090044
Hyphenated Format 0009-0044

Supplemental Identifiers

RxCUI
197782 197783 197787 208680 208712 208816
UPC
0300090044015 0300090031015 0300090012014
UNII
WI4X0X7BPJ
NUI
N0000175576 N0000175450

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name cortef (source: ndc)
Generic Name hydrocortisone (source: ndc)
Application Number NDA008697 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (0009-0044-01)
source: ndc

Packages (1)

0009-0044-01 100 TABLET in 1 BOTTLE (0009-0044-01)

Ingredients (1)

hydrocortisone (20 mg/1)

Linked Drug Pages (1)

CORTEF ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "17306ca2-c631-4281-824c-1cb6d63dcac1", "openfda": {"nui": ["N0000175576", "N0000175450"], "upc": ["0300090044015", "0300090031015", "0300090012014"], "unii": ["WI4X0X7BPJ"], "rxcui": ["197782", "197783", "197787", "208680", "208712", "208816"], "spl_set_id": ["9ce19944-dd88-4a7b-84ca-b07f4ec23bad"], "pharm_class_epc": ["Corticosteroid [EPC]"], "pharm_class_moa": ["Corticosteroid Hormone Receptor Agonists [MoA]"], "manufacturer_name": ["Pharmacia & Upjohn Company LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (0009-0044-01)", "package_ndc": "0009-0044-01", "marketing_start_date": "19521215"}], "brand_name": "CORTEF", "product_id": "0009-0044_17306ca2-c631-4281-824c-1cb6d63dcac1", "dosage_form": "TABLET", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "0009-0044", "generic_name": "hydrocortisone", "labeler_name": "Pharmacia & Upjohn Company LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "CORTEF", "active_ingredients": [{"name": "HYDROCORTISONE", "strength": "20 mg/1"}], "application_number": "NDA008697", "marketing_category": "NDA", "marketing_start_date": "19521215", "listing_expiration_date": "20261231"}