hydrocortisone
Generic: hydrocortisone
Labeler: mylan pharmaceuticals inc.Drug Facts
Product Profile
Brand Name
hydrocortisone
Generic Name
hydrocortisone
Labeler
mylan pharmaceuticals inc.
Dosage Form
TABLET
Routes
Active Ingredients
hydrocortisone 20 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
59762-0075
Product ID
59762-0075_a6ea7547-fb8f-4df1-b5bb-e0f575162d3c
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
NDA AUTHORIZED GENERIC
Application Number
NDA008697
Listing Expiration
2026-12-31
Marketing Start
2013-02-20
Pharmacologic Class
Established (EPC)
Mechanism of Action
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
597620075
Hyphenated Format
59762-0075
Supplemental Identifiers
RxCUI
UPC
UNII
NUI
Packaging Origin
Original Packager
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
hydrocortisone (source: ndc)
Generic Name
hydrocortisone (source: ndc)
Application Number
NDA008697 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 20 mg/1
Packaging
- 100 TABLET in 1 BOTTLE (59762-0075-1)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "a6ea7547-fb8f-4df1-b5bb-e0f575162d3c", "openfda": {"nui": ["N0000175576", "N0000175450"], "upc": ["0359762007414", "0359762007315"], "unii": ["WI4X0X7BPJ"], "rxcui": ["197782", "197783", "197787"], "spl_set_id": ["bc751403-94f2-4f9d-b533-cf6186a40ceb"], "pharm_class_epc": ["Corticosteroid [EPC]"], "pharm_class_moa": ["Corticosteroid Hormone Receptor Agonists [MoA]"], "manufacturer_name": ["Mylan Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (59762-0075-1)", "package_ndc": "59762-0075-1", "marketing_start_date": "20130220"}], "brand_name": "Hydrocortisone", "product_id": "59762-0075_a6ea7547-fb8f-4df1-b5bb-e0f575162d3c", "dosage_form": "TABLET", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "59762-0075", "generic_name": "hydrocortisone", "labeler_name": "Mylan Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hydrocortisone", "active_ingredients": [{"name": "HYDROCORTISONE", "strength": "20 mg/1"}], "application_number": "NDA008697", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20130220", "listing_expiration_date": "20261231"}