dexamethasone
Generic: dexamethasone
Labeler: direct_rxDrug Facts
Product Profile
Brand Name
dexamethasone
Generic Name
dexamethasone
Labeler
direct_rx
Dosage Form
TABLET
Routes
Active Ingredients
dexamethasone .75 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
72189-383
Product ID
72189-383_2c4cd6df-c358-b1f7-e063-6394a90a9507
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA084613
Listing Expiration
2026-12-31
Marketing Start
2022-09-19
Pharmacologic Class
Established (EPC)
Mechanism of Action
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
72189383
Hyphenated Format
72189-383
Supplemental Identifiers
RxCUI
UNII
NUI
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
ANDA084613 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- .75 mg/1
Packaging
- 30 TABLET in 1 BOTTLE (72189-383-30)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2c4cd6df-c358-b1f7-e063-6394a90a9507", "openfda": {"nui": ["N0000175576", "N0000175450"], "unii": ["7S5I7G3JQL"], "rxcui": ["343033"], "spl_set_id": ["e90cb7f5-5e99-fbf3-e053-2995a90a70aa"], "pharm_class_epc": ["Corticosteroid [EPC]"], "pharm_class_moa": ["Corticosteroid Hormone Receptor Agonists [MoA]"], "manufacturer_name": ["Direct_Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (72189-383-30)", "package_ndc": "72189-383-30", "marketing_start_date": "20220919"}], "brand_name": "Dexamethasone", "product_id": "72189-383_2c4cd6df-c358-b1f7-e063-6394a90a9507", "dosage_form": "TABLET", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "72189-383", "generic_name": "Dexamethasone", "labeler_name": "Direct_Rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Dexamethasone", "active_ingredients": [{"name": "DEXAMETHASONE", "strength": ".75 mg/1"}], "application_number": "ANDA084613", "marketing_category": "ANDA", "marketing_start_date": "20220919", "listing_expiration_date": "20261231"}