dexamethasone

Generic: dexamethasone

Labeler: direct rx
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name dexamethasone
Generic Name dexamethasone
Labeler direct rx
Dosage Form TABLET
Routes
ORAL
Active Ingredients

dexamethasone 4 mg/1

Manufacturer
Direct Rx

Identifiers & Regulatory

Product NDC 72189-254
Product ID 72189-254_2c28e5cd-de70-cb2d-e063-6394a90ab7f2
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA084612
Listing Expiration 2026-12-31
Marketing Start 2021-09-20

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 72189254
Hyphenated Format 72189-254

Supplemental Identifiers

RxCUI
197582
UNII
7S5I7G3JQL
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 dexamethasone (source: ndc)
Generic Name dexamethasone (source: ndc)
Application Number ANDA084612 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 4 mg/1
source: ndc
Packaging
  • 10 TABLET in 1 BOTTLE (72189-254-10)
source: ndc

Packages (1)

72189-254-10 10 TABLET in 1 BOTTLE (72189-254-10)

Ingredients (1)

dexamethasone (4 mg/1)

Linked Drug Pages (1)

DEXAMETHASONE ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "2c28e5cd-de70-cb2d-e063-6394a90ab7f2", "openfda": {"nui": ["N0000175576", "N0000175450"], "unii": ["7S5I7G3JQL"], "rxcui": ["197582"], "spl_set_id": ["cc7140de-a205-f675-e053-2995a90ac22b"], "pharm_class_epc": ["Corticosteroid [EPC]"], "pharm_class_moa": ["Corticosteroid Hormone Receptor Agonists [MoA]"], "manufacturer_name": ["Direct Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "10 TABLET in 1 BOTTLE (72189-254-10)", "package_ndc": "72189-254-10", "marketing_start_date": "20210920"}], "brand_name": "DEXAMETHASONE", "product_id": "72189-254_2c28e5cd-de70-cb2d-e063-6394a90ab7f2", "dosage_form": "TABLET", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "72189-254", "generic_name": "DEXAMETHASONE", "labeler_name": "Direct Rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "DEXAMETHASONE", "active_ingredients": [{"name": "DEXAMETHASONE", "strength": "4 mg/1"}], "application_number": "ANDA084612", "marketing_category": "ANDA", "marketing_start_date": "20210920", "listing_expiration_date": "20261231"}