dexamethasone

Generic: dexamethasone

Labeler: preferred pharmaceuticals inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name dexamethasone
Generic Name dexamethasone
Labeler preferred pharmaceuticals inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

dexamethasone 4 mg/1

Manufacturer
Preferred Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 68788-8824
Product ID 68788-8824_b883860c-27ba-4bac-8ae3-4cf4d82d5071
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA217001
Listing Expiration 2026-12-31
Marketing Start 2025-02-10

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 687888824
Hyphenated Format 68788-8824

Supplemental Identifiers

RxCUI
197582
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 ANDA217001 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 4 mg/1
source: ndc
Packaging
  • 12 TABLET in 1 BOTTLE (68788-8824-1)
  • 30 TABLET in 1 BOTTLE (68788-8824-3)
  • 15 TABLET in 1 BOTTLE (68788-8824-5)
  • 6 TABLET in 1 BOTTLE (68788-8824-6)
source: ndc

Packages (4)

Ingredients (1)

dexamethasone (4 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "b883860c-27ba-4bac-8ae3-4cf4d82d5071", "openfda": {"nui": ["N0000175576", "N0000175450"], "unii": ["7S5I7G3JQL"], "rxcui": ["197582"], "spl_set_id": ["b883860c-27ba-4bac-8ae3-4cf4d82d5071"], "pharm_class_epc": ["Corticosteroid [EPC]"], "pharm_class_moa": ["Corticosteroid Hormone Receptor Agonists [MoA]"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "12 TABLET in 1 BOTTLE (68788-8824-1)", "package_ndc": "68788-8824-1", "marketing_start_date": "20250210"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (68788-8824-3)", "package_ndc": "68788-8824-3", "marketing_start_date": "20250210"}, {"sample": false, "description": "15 TABLET in 1 BOTTLE (68788-8824-5)", "package_ndc": "68788-8824-5", "marketing_start_date": "20250210"}, {"sample": false, "description": "6 TABLET in 1 BOTTLE (68788-8824-6)", "package_ndc": "68788-8824-6", "marketing_start_date": "20250210"}], "brand_name": "Dexamethasone", "product_id": "68788-8824_b883860c-27ba-4bac-8ae3-4cf4d82d5071", "dosage_form": "TABLET", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "68788-8824", "generic_name": "Dexamethasone", "labeler_name": "Preferred Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Dexamethasone", "active_ingredients": [{"name": "DEXAMETHASONE", "strength": "4 mg/1"}], "application_number": "ANDA217001", "marketing_category": "ANDA", "marketing_start_date": "20250210", "listing_expiration_date": "20261231"}