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, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

clonidine hydrochloride .1 mg/1

Manufacturer
Actavis Pharma, Inc.

Identifiers & Regulatory

Product NDC 0228-4241
Product ID 0228-4241_5082cfd3-e748-4c4b-81ba-0957f02244a5
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA203320
Listing Expiration 2026-12-31
Marketing Start 2015-06-17

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 02284241
Hyphenated Format 0228-4241

Supplemental Identifiers

RxCUI
1013930
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 ANDA203320 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • .1 mg/1
source: ndc
Packaging
  • 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (0228-4241-06)
source: ndc

Packages (1)

0228-4241-06 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (0228-4241-06)

Ingredients (1)

clonidine hydrochloride (.1 mg/1)

Linked Drug Pages (1)

Clonidine Hydrochloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "5082cfd3-e748-4c4b-81ba-0957f02244a5", "openfda": {"unii": ["W76I6XXF06"], "rxcui": ["1013930"], "spl_set_id": ["0100c70d-7fde-46a1-8374-940550a27e43"], "manufacturer_name": ["Actavis Pharma, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, EXTENDED RELEASE in 1 BOTTLE (0228-4241-06)", "package_ndc": "0228-4241-06", "marketing_start_date": "20150617"}], "brand_name": "Clonidine Hydrochloride", "product_id": "0228-4241_5082cfd3-e748-4c4b-81ba-0957f02244a5", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Adrenergic alpha2-Agonists [MoA]", "Central alpha-2 Adrenergic Agonist [EPC]"], "product_ndc": "0228-4241", "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": ".1 mg/1"}], "application_number": "ANDA203320", "marketing_category": "ANDA", "marketing_start_date": "20150617", "listing_expiration_date": "20261231"}