clonidine hydrochloride

Generic: clonidine hydrochloride

Labeler: aurobindo pharma limited
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name clonidine hydrochloride
Generic Name clonidine hydrochloride
Labeler aurobindo pharma limited
Dosage Form TABLET
Routes
ORAL
Active Ingredients

clonidine hydrochloride .2 mg/1

Manufacturer
Aurobindo Pharma Limited

Identifiers & Regulatory

Product NDC 59651-233
Product ID 59651-233_2b75c20c-9dcc-4a63-854a-e9cdd2d7c1fb
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA070886
Listing Expiration 2026-12-31
Marketing Start 2021-06-02

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 59651233
Hyphenated Format 59651-233

Supplemental Identifiers

RxCUI
884173 884185 884189
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 ANDA070886 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • .2 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (59651-233-01)
  • 500 TABLET in 1 BOTTLE (59651-233-05)
source: ndc

Packages (2)

59651-233-01 100 TABLET in 1 BOTTLE (59651-233-01) 59651-233-05 500 TABLET in 1 BOTTLE (59651-233-05)

Ingredients (1)

clonidine hydrochloride (.2 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": "2b75c20c-9dcc-4a63-854a-e9cdd2d7c1fb", "openfda": {"unii": ["W76I6XXF06"], "rxcui": ["884173", "884185", "884189"], "spl_set_id": ["2b75c20c-9dcc-4a63-854a-e9cdd2d7c1fb"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (59651-233-01)", "package_ndc": "59651-233-01", "marketing_start_date": "20210602"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (59651-233-05)", "package_ndc": "59651-233-05", "marketing_start_date": "20210602"}], "brand_name": "Clonidine Hydrochloride", "product_id": "59651-233_2b75c20c-9dcc-4a63-854a-e9cdd2d7c1fb", "dosage_form": "TABLET", "pharm_class": ["Adrenergic alpha2-Agonists [MoA]", "Central alpha-2 Adrenergic Agonist [EPC]"], "product_ndc": "59651-233", "generic_name": "Clonidine Hydrochloride", "labeler_name": "Aurobindo Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Clonidine Hydrochloride", "active_ingredients": [{"name": "CLONIDINE HYDROCHLORIDE", "strength": ".2 mg/1"}], "application_number": "ANDA070886", "marketing_category": "ANDA", "marketing_start_date": "20210602", "listing_expiration_date": "20261231"}