clonidine hydrochloride

Generic: clonidine hydrochloride

Labeler: bluepoint laboratories
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name clonidine hydrochloride
Generic Name clonidine hydrochloride
Labeler bluepoint laboratories
Dosage Form TABLET
Routes
ORAL
Active Ingredients

clonidine hydrochloride .2 mg/1

Manufacturer
BluePoint Laboratories

Identifiers & Regulatory

Product NDC 68001-238
Product ID 68001-238_42c4b1f4-a2c5-e21f-e063-6294a90aa481
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 68001238
Hyphenated Format 68001-238

Supplemental Identifiers

RxCUI
884173 884185 884189
UPC
0368001239004 0368001238007 0368001237000
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 (68001-238-00)
  • 500 TABLET in 1 BOTTLE (68001-238-03)
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": "42c4b1f4-a2c5-e21f-e063-6294a90aa481", "openfda": {"upc": ["0368001239004", "0368001238007", "0368001237000"], "unii": ["W76I6XXF06"], "rxcui": ["884173", "884185", "884189"], "spl_set_id": ["1ea412db-d847-4094-be83-e3bd7328537a"], "manufacturer_name": ["BluePoint Laboratories"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (68001-238-00)", "package_ndc": "68001-238-00", "marketing_start_date": "19950103"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (68001-238-03)", "package_ndc": "68001-238-03", "marketing_start_date": "19950103"}], "brand_name": "Clonidine Hydrochloride", "product_id": "68001-238_42c4b1f4-a2c5-e21f-e063-6294a90aa481", "dosage_form": "TABLET", "pharm_class": ["Adrenergic alpha2-Agonists [MoA]", "Central alpha-2 Adrenergic Agonist [EPC]"], "product_ndc": "68001-238", "generic_name": "Clonidine Hydrochloride", "labeler_name": "BluePoint Laboratories", "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"}