dexamethasone
Generic: dexamethasone
Labeler: pd-rx pharmaceuticals, inc.Drug Facts
Product Profile
Brand Name
dexamethasone
Generic Name
dexamethasone
Labeler
pd-rx pharmaceuticals, inc.
Dosage Form
TABLET
Routes
Active Ingredients
dexamethasone 2 mg/1
Manufacturer
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)
Mechanism of Action
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
43063266
Hyphenated Format
43063-266
Supplemental Identifiers
RxCUI
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
ANDA087916 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 2 mg/1
Packaging
- 7 TABLET in 1 BOTTLE, PLASTIC (43063-266-07)
Packages (1)
Ingredients (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"}