hydrocortisone

Generic: hydrocortisone

Labeler: pd-rx pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name hydrocortisone
Generic Name hydrocortisone
Labeler pd-rx pharmaceuticals, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

hydrocortisone 20 mg/1

Manufacturer
PD-Rx Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 72789-229
Product ID 72789-229_4bac06f7-513b-6b33-e063-6394a90a0b43
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA207029
Listing Expiration 2027-12-31
Marketing Start 2021-12-22

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 72789229
Hyphenated Format 72789-229

Supplemental Identifiers

RxCUI
197782 197783 197787
UPC
0372789229010 0372789227504 0372789228013
UNII
WI4X0X7BPJ
NUI
N0000175576 N0000175450

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 ANDA207029 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE, PLASTIC (72789-229-01)
source: ndc

Packages (1)

72789-229-01 100 TABLET in 1 BOTTLE, PLASTIC (72789-229-01)

Ingredients (1)

hydrocortisone (20 mg/1)

Linked Drug Pages (1)

Hydrocortisone ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "4bac06f7-513b-6b33-e063-6394a90a0b43", "openfda": {"nui": ["N0000175576", "N0000175450"], "upc": ["0372789229010", "0372789227504", "0372789228013"], "unii": ["WI4X0X7BPJ"], "rxcui": ["197782", "197783", "197787"], "spl_set_id": ["931ed426-89a1-4877-a4a5-cb963d51e717"], "pharm_class_epc": ["Corticosteroid [EPC]"], "pharm_class_moa": ["Corticosteroid Hormone Receptor Agonists [MoA]"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (72789-229-01)", "package_ndc": "72789-229-01", "marketing_start_date": "20221222"}], "brand_name": "Hydrocortisone", "product_id": "72789-229_4bac06f7-513b-6b33-e063-6394a90a0b43", "dosage_form": "TABLET", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "72789-229", "generic_name": "Hydrocortisone", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hydrocortisone", "active_ingredients": [{"name": "HYDROCORTISONE", "strength": "20 mg/1"}], "application_number": "ANDA207029", "marketing_category": "ANDA", "marketing_start_date": "20211222", "listing_expiration_date": "20271231"}