dexamethasone

Generic: dexamethasone

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

Drug Facts

Product Profile

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

dexamethasone 2 mg/1

Manufacturer
Doc Rx

Identifiers & Regulatory

Product NDC 69306-112
Product ID 69306-112_c479d9ec-ec8d-7228-e053-2a95a90a9644
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA087916
Listing Expiration 2026-12-31
Marketing Start 1982-08-26

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 69306112
Hyphenated Format 69306-112

Supplemental Identifiers

RxCUI
197579 197581 197582
UPC
0369306111606 0369306112306 0369306114065
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 ANDA087916 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 2 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE, PLASTIC (69306-112-30)
source: ndc

Packages (1)

69306-112-30 30 TABLET in 1 BOTTLE, PLASTIC (69306-112-30)

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": "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": "30 TABLET in 1 BOTTLE, PLASTIC (69306-112-30)", "package_ndc": "69306-112-30", "marketing_start_date": "20200625"}], "brand_name": "Dexamethasone", "product_id": "69306-112_c479d9ec-ec8d-7228-e053-2a95a90a9644", "dosage_form": "TABLET", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "69306-112", "generic_name": "Dexamethasone", "labeler_name": "Doc Rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Dexamethasone", "active_ingredients": [{"name": "DEXAMETHASONE", "strength": "2 mg/1"}], "application_number": "ANDA087916", "marketing_category": "ANDA", "marketing_start_date": "19820826", "listing_expiration_date": "20261231"}