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 2 mg/1

Manufacturer
Direct_Rx

Identifiers & Regulatory

Product NDC 72189-523
Product ID 72189-523_4a2b20b5-96c9-0373-e063-6294a90a7e5e
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA217696
Listing Expiration 2027-12-31
Marketing Start 2023-11-13

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 72189523
Hyphenated Format 72189-523

Supplemental Identifiers

RxCUI
197581
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 ANDA217696 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 2 mg/1
source: ndc
Packaging
  • 8 TABLET in 1 BOTTLE (72189-523-08)
  • 15 TABLET in 1 BOTTLE (72189-523-15)
source: ndc

Packages (2)

72189-523-08 8 TABLET in 1 BOTTLE (72189-523-08) 72189-523-15 15 TABLET in 1 BOTTLE (72189-523-15)

Ingredients (1)

dexamethasone (2 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": "4a2b20b5-96c9-0373-e063-6294a90a7e5e", "openfda": {"nui": ["N0000175576", "N0000175450"], "unii": ["7S5I7G3JQL"], "rxcui": ["197581"], "spl_set_id": ["0a0db8e7-8474-3d08-e063-6294a90af3f5"], "pharm_class_epc": ["Corticosteroid [EPC]"], "pharm_class_moa": ["Corticosteroid Hormone Receptor Agonists [MoA]"], "manufacturer_name": ["Direct_Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "8 TABLET in 1 BOTTLE (72189-523-08)", "package_ndc": "72189-523-08", "marketing_start_date": "20231113"}, {"sample": false, "description": "15 TABLET in 1 BOTTLE (72189-523-15)", "package_ndc": "72189-523-15", "marketing_start_date": "20231113"}], "brand_name": "Dexamethasone", "product_id": "72189-523_4a2b20b5-96c9-0373-e063-6294a90a7e5e", "dosage_form": "TABLET", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "72189-523", "generic_name": "Dexamethasone", "labeler_name": "Direct_Rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Dexamethasone", "active_ingredients": [{"name": "DEXAMETHASONE", "strength": "2 mg/1"}], "application_number": "ANDA217696", "marketing_category": "ANDA", "marketing_start_date": "20231113", "listing_expiration_date": "20271231"}