clonidine hydrochloride

Generic: clonidine hydrochloride

Labeler: nucare pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

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

clonidine hydrochloride .1 mg/1

Manufacturer
NuCare Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 66267-061
Product ID 66267-061_1f98d40a-8eba-1de2-e063-6394a90aa38b
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA078895
Listing Expiration 2026-12-31
Marketing Start 2009-09-21

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 66267061
Hyphenated Format 66267-061

Supplemental Identifiers

RxCUI
884173
UPC
0366267061902
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 ANDA078895 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • .1 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE, PLASTIC (66267-061-30)
  • 60 TABLET in 1 BOTTLE, PLASTIC (66267-061-60)
  • 90 TABLET in 1 BOTTLE, PLASTIC (66267-061-90)
source: ndc

Packages (3)

66267-061-30 30 TABLET in 1 BOTTLE, PLASTIC (66267-061-30) 66267-061-60 60 TABLET in 1 BOTTLE, PLASTIC (66267-061-60) 66267-061-90 90 TABLET in 1 BOTTLE, PLASTIC (66267-061-90)

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": "1f98d40a-8eba-1de2-e063-6394a90aa38b", "openfda": {"upc": ["0366267061902"], "unii": ["W76I6XXF06"], "rxcui": ["884173"], "spl_set_id": ["3d966e77-9331-4051-e054-00144ff8d46c"], "manufacturer_name": ["NuCare Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (66267-061-30)", "package_ndc": "66267-061-30", "marketing_start_date": "20160928"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE, PLASTIC (66267-061-60)", "package_ndc": "66267-061-60", "marketing_start_date": "20160928"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (66267-061-90)", "package_ndc": "66267-061-90", "marketing_start_date": "20160928"}], "brand_name": "clonidine hydrochloride", "product_id": "66267-061_1f98d40a-8eba-1de2-e063-6394a90aa38b", "dosage_form": "TABLET", "pharm_class": ["Adrenergic alpha2-Agonists [MoA]", "Central alpha-2 Adrenergic Agonist [EPC]"], "product_ndc": "66267-061", "generic_name": "clonidine hydrochloride", "labeler_name": "NuCare Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "clonidine hydrochloride", "active_ingredients": [{"name": "CLONIDINE HYDROCHLORIDE", "strength": ".1 mg/1"}], "application_number": "ANDA078895", "marketing_category": "ANDA", "marketing_start_date": "20090921", "listing_expiration_date": "20261231"}