dexamethasone
Generic: dexamethasone
Labeler: doc rxDrug Facts
Product Profile
Brand Name
dexamethasone
Generic Name
dexamethasone
Labeler
doc rx
Dosage Form
TABLET
Routes
Active Ingredients
dexamethasone 4 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
69306-114
Product ID
69306-114_c479d9ec-ec8d-7228-e053-2a95a90a9644
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA084612
Listing Expiration
2026-12-31
Marketing Start
1978-07-19
Pharmacologic Class
Established (EPC)
Mechanism of Action
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
69306114
Hyphenated Format
69306-114
Supplemental Identifiers
RxCUI
UPC
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
ANDA084612 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 4 mg/1
Packaging
- 6 TABLET in 1 BOTTLE, PLASTIC (69306-114-06)
- 30 TABLET in 1 BOTTLE, PLASTIC (69306-114-30)
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "c479d9ec-ec8d-7228-e053-2a95a90a9644", "openfda": {"nui": ["N0000175576", "N0000175450"], "upc": ["0369306111606", "0369306112306", "0369306114065"], "unii": ["7S5I7G3JQL"], "rxcui": ["197579", "197581", "197582"], "spl_set_id": ["f1c30431-554b-4161-9d8c-5795c689e0bd"], "pharm_class_epc": ["Corticosteroid [EPC]"], "pharm_class_moa": ["Corticosteroid Hormone Receptor Agonists [MoA]"], "manufacturer_name": ["Doc Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "6 TABLET in 1 BOTTLE, PLASTIC (69306-114-06)", "package_ndc": "69306-114-06", "marketing_start_date": "20201008"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (69306-114-30)", "package_ndc": "69306-114-30", "marketing_start_date": "20200701"}], "brand_name": "Dexamethasone", "product_id": "69306-114_c479d9ec-ec8d-7228-e053-2a95a90a9644", "dosage_form": "TABLET", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "69306-114", "generic_name": "Dexamethasone", "labeler_name": "Doc 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": "19780719", "listing_expiration_date": "20261231"}