clonidine hydrochloride

Generic: clonidine hydrochloride

Labeler: asclemed usa, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

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

clonidine hydrochloride .1 mg/1

Manufacturer
Asclemed USA, Inc.

Identifiers & Regulatory

Product NDC 76420-066
Product ID 76420-066_b26a7261-c68e-834b-e053-2a95a90a1f7d
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA091368
Listing Expiration 2026-12-31
Marketing Start 2016-05-03

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 76420066
Hyphenated Format 76420-066

Supplemental Identifiers

RxCUI
884173
UNII
W76I6XXF06

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 ANDA091368 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • .1 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (76420-066-01)
  • 20 TABLET in 1 BOTTLE (76420-066-20)
  • 30 TABLET in 1 BOTTLE (76420-066-30)
  • 60 TABLET in 1 BOTTLE (76420-066-60)
  • 90 TABLET in 1 BOTTLE (76420-066-90)
source: ndc

Packages (5)

76420-066-01 100 TABLET in 1 BOTTLE (76420-066-01) 76420-066-20 20 TABLET in 1 BOTTLE (76420-066-20) 76420-066-30 30 TABLET in 1 BOTTLE (76420-066-30) 76420-066-60 60 TABLET in 1 BOTTLE (76420-066-60) 76420-066-90 90 TABLET in 1 BOTTLE (76420-066-90)

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": "b26a7261-c68e-834b-e053-2a95a90a1f7d", "openfda": {"unii": ["W76I6XXF06"], "rxcui": ["884173"], "spl_set_id": ["b60034a6-b8ba-4e54-9ef0-029965e67bc0"], "manufacturer_name": ["Asclemed USA, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (76420-066-01)", "package_ndc": "76420-066-01", "marketing_start_date": "20201024"}, {"sample": false, "description": "20 TABLET in 1 BOTTLE (76420-066-20)", "package_ndc": "76420-066-20", "marketing_start_date": "20201024"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (76420-066-30)", "package_ndc": "76420-066-30", "marketing_start_date": "20201024"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (76420-066-60)", "package_ndc": "76420-066-60", "marketing_start_date": "20201024"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (76420-066-90)", "package_ndc": "76420-066-90", "marketing_start_date": "20201024"}], "brand_name": "clonidine hydrochloride", "product_id": "76420-066_b26a7261-c68e-834b-e053-2a95a90a1f7d", "dosage_form": "TABLET", "pharm_class": ["Adrenergic alpha2-Agonists [MoA]", "Central alpha-2 Adrenergic Agonist [EPC]"], "product_ndc": "76420-066", "generic_name": "Clonidine Hydrochloride", "labeler_name": "Asclemed USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "clonidine hydrochloride", "active_ingredients": [{"name": "CLONIDINE HYDROCHLORIDE", "strength": ".1 mg/1"}], "application_number": "ANDA091368", "marketing_category": "ANDA", "marketing_start_date": "20160503", "listing_expiration_date": "20261231"}