clonidine hydrochloride

Generic: clonidine hydrochloride

Labeler: actavis pharma, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name clonidine hydrochloride
Generic Name clonidine hydrochloride
Labeler actavis pharma, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

clonidine hydrochloride .2 mg/1

Manufacturer
Actavis Pharma, Inc.

Identifiers & Regulatory

Product NDC 0228-2128
Product ID 0228-2128_860129c9-0bba-471e-a90c-b6bede1833b8
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA070975
Listing Expiration 2026-12-31
Marketing Start 1995-01-03

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 02282128
Hyphenated Format 0228-2128

Supplemental Identifiers

RxCUI
884173 884185 884189
UPC
0302282128107 0302282129104 0302282127100
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 hydrochloride (source: ndc)
Generic Name clonidine hydrochloride (source: ndc)
Application Number ANDA070975 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • .2 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (0228-2128-10)
  • 500 TABLET in 1 BOTTLE (0228-2128-50)
source: ndc

Packages (2)

Ingredients (1)

clonidine hydrochloride (.2 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "860129c9-0bba-471e-a90c-b6bede1833b8", "openfda": {"upc": ["0302282128107", "0302282129104", "0302282127100"], "unii": ["W76I6XXF06"], "rxcui": ["884173", "884185", "884189"], "spl_set_id": ["a842ab83-3531-44dd-a8a8-64dd89e87026"], "manufacturer_name": ["Actavis Pharma, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (0228-2128-10)", "package_ndc": "0228-2128-10", "marketing_start_date": "19950103"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (0228-2128-50)", "package_ndc": "0228-2128-50", "marketing_start_date": "19950103"}], "brand_name": "Clonidine Hydrochloride", "product_id": "0228-2128_860129c9-0bba-471e-a90c-b6bede1833b8", "dosage_form": "TABLET", "pharm_class": ["Adrenergic alpha2-Agonists [MoA]", "Central alpha-2 Adrenergic Agonist [EPC]"], "product_ndc": "0228-2128", "generic_name": "Clonidine Hydrochloride", "labeler_name": "Actavis Pharma, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Clonidine Hydrochloride", "active_ingredients": [{"name": "CLONIDINE HYDROCHLORIDE", "strength": ".2 mg/1"}], "application_number": "ANDA070975", "marketing_category": "ANDA", "marketing_start_date": "19950103", "listing_expiration_date": "20261231"}