clonidine hydrochloride

Generic: clonidine hydrochloride

Labeler: trupharma, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name clonidine hydrochloride
Generic Name clonidine hydrochloride
Labeler trupharma, llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

clonidine hydrochloride .2 mg/1

Manufacturer
TruPharma, LLC

Identifiers & Regulatory

Product NDC 52817-181
Product ID 52817-181_2a9f317f-73f5-82d5-e063-6394a90a45bb
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA070924
Listing Expiration 2026-12-31
Marketing Start 2017-06-01

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 52817181
Hyphenated Format 52817-181

Supplemental Identifiers

RxCUI
884173 884185 884189
UPC
0352817181107 0352817182005 0352817180100 0352817182104
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 ANDA070924 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • .2 mg/1
source: ndc
Packaging
  • 1000 TABLET in 1 BOTTLE (52817-181-00)
  • 100 TABLET in 1 BOTTLE (52817-181-10)
  • 500 TABLET in 1 BOTTLE (52817-181-50)
source: ndc

Packages (3)

52817-181-00 1000 TABLET in 1 BOTTLE (52817-181-00) 52817-181-10 100 TABLET in 1 BOTTLE (52817-181-10) 52817-181-50 500 TABLET in 1 BOTTLE (52817-181-50)

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": "2a9f317f-73f5-82d5-e063-6394a90a45bb", "openfda": {"upc": ["0352817181107", "0352817182005", "0352817180100", "0352817182104"], "unii": ["W76I6XXF06"], "rxcui": ["884173", "884185", "884189"], "spl_set_id": ["c83e4e4f-bd0e-449d-958a-dc0d570a01ba"], "manufacturer_name": ["TruPharma, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET in 1 BOTTLE (52817-181-00)", "package_ndc": "52817-181-00", "marketing_start_date": "20170601"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (52817-181-10)", "package_ndc": "52817-181-10", "marketing_start_date": "20170601"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (52817-181-50)", "package_ndc": "52817-181-50", "marketing_start_date": "20170601"}], "brand_name": "Clonidine hydrochloride", "product_id": "52817-181_2a9f317f-73f5-82d5-e063-6394a90a45bb", "dosage_form": "TABLET", "pharm_class": ["Adrenergic alpha2-Agonists [MoA]", "Central alpha-2 Adrenergic Agonist [EPC]"], "product_ndc": "52817-181", "generic_name": "Clonidine hydrochloride", "labeler_name": "TruPharma, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Clonidine hydrochloride", "active_ingredients": [{"name": "CLONIDINE HYDROCHLORIDE", "strength": ".2 mg/1"}], "application_number": "ANDA070924", "marketing_category": "ANDA", "marketing_start_date": "20170601", "listing_expiration_date": "20261231"}