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 1.5 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
72189-468
Product ID
72189-468_2c4deb3e-a1c6-75c0-e063-6394a90a9cb7
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA215604
Listing Expiration
2026-12-31
Marketing Start
2023-05-04
Pharmacologic Class
Established (EPC)
Mechanism of Action
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
72189468
Hyphenated Format
72189-468
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
ANDA215604 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 1.5 mg/1
Packaging
- 15 TABLET in 1 BOTTLE (72189-468-15)
- 21 TABLET in 1 BOTTLE (72189-468-21)
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2c4deb3e-a1c6-75c0-e063-6394a90a9cb7", "openfda": {"nui": ["N0000175576", "N0000175450"], "unii": ["7S5I7G3JQL"], "rxcui": ["197580"], "spl_set_id": ["fade983c-81fb-df94-e053-6394a90a7560"], "pharm_class_epc": ["Corticosteroid [EPC]"], "pharm_class_moa": ["Corticosteroid Hormone Receptor Agonists [MoA]"], "manufacturer_name": ["Direct_Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "15 TABLET in 1 BOTTLE (72189-468-15)", "package_ndc": "72189-468-15", "marketing_start_date": "20230504"}, {"sample": false, "description": "21 TABLET in 1 BOTTLE (72189-468-21)", "package_ndc": "72189-468-21", "marketing_start_date": "20230504"}], "brand_name": "Dexamethasone", "product_id": "72189-468_2c4deb3e-a1c6-75c0-e063-6394a90a9cb7", "dosage_form": "TABLET", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "72189-468", "generic_name": "Dexamethasone", "labeler_name": "Direct_Rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Dexamethasone", "active_ingredients": [{"name": "DEXAMETHASONE", "strength": "1.5 mg/1"}], "application_number": "ANDA215604", "marketing_category": "ANDA", "marketing_start_date": "20230504", "listing_expiration_date": "20261231"}