clonidine hydrochloride

Generic: clonidine hydrochloride

Labeler: proficient rx lp
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name clonidine hydrochloride
Generic Name clonidine hydrochloride
Labeler proficient rx lp
Dosage Form TABLET
Routes
ORAL
Active Ingredients

clonidine hydrochloride .2 mg/1

Manufacturer
Proficient Rx LP

Identifiers & Regulatory

Product NDC 71205-218
Product ID 71205-218_562b6948-1bb6-4129-adb1-3b33c4b14d3e
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 71205218
Hyphenated Format 71205-218

Supplemental Identifiers

RxCUI
884185
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
  • .2 mg/1
source: ndc
Packaging
  • 20 TABLET in 1 BOTTLE, PLASTIC (71205-218-20)
  • 30 TABLET in 1 BOTTLE, PLASTIC (71205-218-30)
  • 60 TABLET in 1 BOTTLE, PLASTIC (71205-218-60)
  • 90 TABLET in 1 BOTTLE, PLASTIC (71205-218-90)
source: ndc

Packages (4)

71205-218-20 20 TABLET in 1 BOTTLE, PLASTIC (71205-218-20) 71205-218-30 30 TABLET in 1 BOTTLE, PLASTIC (71205-218-30) 71205-218-60 60 TABLET in 1 BOTTLE, PLASTIC (71205-218-60) 71205-218-90 90 TABLET in 1 BOTTLE, PLASTIC (71205-218-90)

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": "562b6948-1bb6-4129-adb1-3b33c4b14d3e", "openfda": {"unii": ["W76I6XXF06"], "rxcui": ["884185"], "spl_set_id": ["c812012c-4b1d-40a4-8d4e-aaae2bf1c852"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET in 1 BOTTLE, PLASTIC (71205-218-20)", "package_ndc": "71205-218-20", "marketing_start_date": "20190201"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (71205-218-30)", "package_ndc": "71205-218-30", "marketing_start_date": "20190201"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE, PLASTIC (71205-218-60)", "package_ndc": "71205-218-60", "marketing_start_date": "20190201"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (71205-218-90)", "package_ndc": "71205-218-90", "marketing_start_date": "20190201"}], "brand_name": "clonidine hydrochloride", "product_id": "71205-218_562b6948-1bb6-4129-adb1-3b33c4b14d3e", "dosage_form": "TABLET", "pharm_class": ["Adrenergic alpha2-Agonists [MoA]", "Central alpha-2 Adrenergic Agonist [EPC]"], "product_ndc": "71205-218", "generic_name": "clonidine hydrochloride", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "clonidine hydrochloride", "active_ingredients": [{"name": "CLONIDINE HYDROCHLORIDE", "strength": ".2 mg/1"}], "application_number": "ANDA078895", "marketing_category": "ANDA", "marketing_start_date": "20090921", "listing_expiration_date": "20261231"}