clonidine hydrochloride

Generic: clonidine hydrochloride

Labeler: directrx
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

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

clonidine hydrochloride .1 mg/1

Manufacturer
DirectRX

Identifiers & Regulatory

Product NDC 61919-605
Product ID 61919-605_0e883a0f-ef15-109e-e063-6294a90aa908
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA091368
Listing Expiration 2026-12-31
Marketing Start 2019-04-04

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 61919605
Hyphenated Format 61919-605

Supplemental Identifiers

RxCUI
884173 884189
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
  • 30 TABLET in 1 BOTTLE (61919-605-30)
  • 60 TABLET in 1 BOTTLE (61919-605-60)
  • 90 TABLET in 1 BOTTLE (61919-605-90)
source: ndc

Packages (3)

61919-605-30 30 TABLET in 1 BOTTLE (61919-605-30) 61919-605-60 60 TABLET in 1 BOTTLE (61919-605-60) 61919-605-90 90 TABLET in 1 BOTTLE (61919-605-90)

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": "0e883a0f-ef15-109e-e063-6294a90aa908", "openfda": {"unii": ["W76I6XXF06"], "rxcui": ["884173", "884189"], "spl_set_id": ["2823a922-3217-6062-e054-00144ff88e88"], "manufacturer_name": ["DirectRX"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (61919-605-30)", "package_ndc": "61919-605-30", "marketing_start_date": "20190404"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (61919-605-60)", "package_ndc": "61919-605-60", "marketing_start_date": "20190404"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (61919-605-90)", "package_ndc": "61919-605-90", "marketing_start_date": "20190404"}], "brand_name": "CLONIDINE HYDROCHLORIDE", "product_id": "61919-605_0e883a0f-ef15-109e-e063-6294a90aa908", "dosage_form": "TABLET", "pharm_class": ["Adrenergic alpha2-Agonists [MoA]", "Central alpha-2 Adrenergic Agonist [EPC]"], "product_ndc": "61919-605", "generic_name": "CLONIDINE HYDROCHLORIDE", "labeler_name": "DirectRX", "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": "20190404", "listing_expiration_date": "20261231"}