clonidine

Generic: clonidine

Labeler: xgen pharmaceuticals djb, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name clonidine
Generic Name clonidine
Labeler xgen pharmaceuticals djb, inc.
Dosage Form INJECTION, SOLUTION
Routes
EPIDURAL
Active Ingredients

clonidine hydrochloride 500 ug/mL

Manufacturer
XGen Pharmaceuticals DJB, Inc.

Identifiers & Regulatory

Product NDC 39822-2010
Product ID 39822-2010_103027a7-2f0d-8d8c-e063-6294a90aedc7
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA203167
Listing Expiration 2026-12-31
Marketing Start 2013-10-29

Pharmacologic Class

Classes
adrenergic alpha2-agonists [moa] central alpha-2 adrenergic agonist [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 398222010
Hyphenated Format 39822-2010

Supplemental Identifiers

RxCUI
884221 884225
UNII
W76I6XXF06

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 clonidine (source: ndc)
Generic Name clonidine (source: ndc)
Application Number ANDA203167 (source: ndc)
Routes
EPIDURAL
source: ndc

Resolved Composition

Strengths
  • 500 ug/mL
source: ndc
Packaging
  • 10 mL in 1 VIAL, SINGLE-DOSE (39822-2010-1)
source: ndc

Packages (1)

Ingredients (1)

clonidine hydrochloride (500 ug/mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["EPIDURAL"], "spl_id": "103027a7-2f0d-8d8c-e063-6294a90aedc7", "openfda": {"unii": ["W76I6XXF06"], "rxcui": ["884221", "884225"], "spl_set_id": ["ada02f1f-ae78-4435-879e-492ae862d504"], "manufacturer_name": ["XGen Pharmaceuticals DJB, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 mL in 1 VIAL, SINGLE-DOSE (39822-2010-1)", "package_ndc": "39822-2010-1", "marketing_start_date": "20131029"}], "brand_name": "Clonidine", "product_id": "39822-2010_103027a7-2f0d-8d8c-e063-6294a90aedc7", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Adrenergic alpha2-Agonists [MoA]", "Central alpha-2 Adrenergic Agonist [EPC]"], "product_ndc": "39822-2010", "generic_name": "Clonidine", "labeler_name": "XGen Pharmaceuticals DJB, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Clonidine", "active_ingredients": [{"name": "CLONIDINE HYDROCHLORIDE", "strength": "500 ug/mL"}], "application_number": "ANDA203167", "marketing_category": "ANDA", "marketing_start_date": "20131029", "listing_expiration_date": "20261231"}