dexamethasone

Generic: dexamethasone

Labeler: pd-rx pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name dexamethasone
Generic Name dexamethasone
Labeler pd-rx pharmaceuticals, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

dexamethasone 2 mg/1

Manufacturer
PD-Rx Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 43063-266
Product ID 43063-266_4137927a-c11c-b316-e063-6294a90a7ca7
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 43063266
Hyphenated Format 43063-266

Supplemental Identifiers

RxCUI
197581
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
  • 7 TABLET in 1 BOTTLE, PLASTIC (43063-266-07)
source: ndc

Packages (1)

Ingredients (1)

dexamethasone (2 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4137927a-c11c-b316-e063-6294a90a7ca7", "openfda": {"nui": ["N0000175576", "N0000175450"], "unii": ["7S5I7G3JQL"], "rxcui": ["197581"], "spl_set_id": ["2ceb3a01-f5bb-4538-b5c1-cea400901d02"], "pharm_class_epc": ["Corticosteroid [EPC]"], "pharm_class_moa": ["Corticosteroid Hormone Receptor Agonists [MoA]"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "7 TABLET in 1 BOTTLE, PLASTIC (43063-266-07)", "package_ndc": "43063-266-07", "marketing_start_date": "20100803"}], "brand_name": "Dexamethasone", "product_id": "43063-266_4137927a-c11c-b316-e063-6294a90a7ca7", "dosage_form": "TABLET", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "43063-266", "generic_name": "Dexamethasone", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "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"}