dexamethasone

Generic: dexamethasone

Labeler: apotex corp.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name dexamethasone
Generic Name dexamethasone
Labeler apotex corp.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

dexamethasone 1 mg/1

Manufacturer
Apotex Corp.

Identifiers & Regulatory

Product NDC 60505-6251
Product ID 60505-6251_4267b6d1-37d3-7ed2-7a89-251185401d0d
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA217695
Listing Expiration 2026-12-31
Marketing Start 2023-11-01

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 605056251
Hyphenated Format 60505-6251

Supplemental Identifiers

RxCUI
197577 197579 197580 197581 197582 197583 343033
UPC
0360505624911 0360505625314 0360505625116 0360505625512 0360505625413 0360505625215 0360505625017
UNII
7S5I7G3JQL
NUI
N0000175576 N0000175450

Packaging Origin

Original Packager
true

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 ANDA217695 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (60505-6251-1)
source: ndc

Packages (1)

60505-6251-1 100 TABLET in 1 BOTTLE (60505-6251-1)

Ingredients (1)

dexamethasone (1 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": "4267b6d1-37d3-7ed2-7a89-251185401d0d", "openfda": {"nui": ["N0000175576", "N0000175450"], "upc": ["0360505624911", "0360505625314", "0360505625116", "0360505625512", "0360505625413", "0360505625215", "0360505625017"], "unii": ["7S5I7G3JQL"], "rxcui": ["197577", "197579", "197580", "197581", "197582", "197583", "343033"], "spl_set_id": ["bfaa71cb-e517-8d94-f64b-8cdbf7b8fbf2"], "pharm_class_epc": ["Corticosteroid [EPC]"], "pharm_class_moa": ["Corticosteroid Hormone Receptor Agonists [MoA]"], "manufacturer_name": ["Apotex Corp."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (60505-6251-1)", "package_ndc": "60505-6251-1", "marketing_start_date": "20231101"}], "brand_name": "Dexamethasone", "product_id": "60505-6251_4267b6d1-37d3-7ed2-7a89-251185401d0d", "dosage_form": "TABLET", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "60505-6251", "generic_name": "Dexamethasone", "labeler_name": "Apotex Corp.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Dexamethasone", "active_ingredients": [{"name": "DEXAMETHASONE", "strength": "1 mg/1"}], "application_number": "ANDA217695", "marketing_category": "ANDA", "marketing_start_date": "20231101", "listing_expiration_date": "20261231"}