clonidine hydrochloride

Generic: clonidine hydrochloride

Labeler: coupler llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

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

clonidine hydrochloride .2 mg/1

Manufacturer
Coupler LLC

Identifiers & Regulatory

Product NDC 67046-1552
Product ID 67046-1552_325f3322-07e7-062c-e063-6394a90aafe2
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA202297
Listing Expiration 2026-12-31
Marketing Start 2025-04-09

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 670461552
Hyphenated Format 67046-1552

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 ANDA202297 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • .2 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BLISTER PACK (67046-1552-3)
source: ndc

Packages (1)

Ingredients (1)

clonidine hydrochloride (.2 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "325f3322-07e7-062c-e063-6394a90aafe2", "openfda": {"unii": ["W76I6XXF06"], "rxcui": ["884185"], "spl_set_id": ["325f382b-6c04-2608-e063-6394a90a3872"], "manufacturer_name": ["Coupler LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (67046-1552-3)", "package_ndc": "67046-1552-3", "marketing_start_date": "20250409"}], "brand_name": "Clonidine Hydrochloride", "product_id": "67046-1552_325f3322-07e7-062c-e063-6394a90aafe2", "dosage_form": "TABLET", "pharm_class": ["Adrenergic alpha2-Agonists [MoA]", "Central alpha-2 Adrenergic Agonist [EPC]"], "product_ndc": "67046-1552", "generic_name": "Clonidine Hydrochloride", "labeler_name": "Coupler LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Clonidine Hydrochloride", "active_ingredients": [{"name": "CLONIDINE HYDROCHLORIDE", "strength": ".2 mg/1"}], "application_number": "ANDA202297", "marketing_category": "ANDA", "marketing_start_date": "20250409", "listing_expiration_date": "20261231"}