clonidine hydrochloride

Generic: clonidine hydrochloride

Labeler: major pharmaceuticals
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

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

clonidine hydrochloride .2 mg/1

Manufacturer
Major Pharmaceuticals

Identifiers & Regulatory

Product NDC 0904-7443
Product ID 0904-7443_7edda115-1bfd-4d8c-a3cd-2c8492ba56cb
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA077901
Listing Expiration 2026-12-31
Marketing Start 2025-11-21

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 09047443
Hyphenated Format 0904-7443

Supplemental Identifiers

RxCUI
884173 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 ANDA077901 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • .2 mg/1
source: ndc
Packaging
  • 100 BLISTER PACK in 1 CARTON (0904-7443-61) / 1 TABLET in 1 BLISTER PACK
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": "7edda115-1bfd-4d8c-a3cd-2c8492ba56cb", "openfda": {"unii": ["W76I6XXF06"], "rxcui": ["884173", "884185"], "spl_set_id": ["8171776a-dd14-4dcc-8860-3c27d8ea9504"], "manufacturer_name": ["Major Pharmaceuticals"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 CARTON (0904-7443-61)  / 1 TABLET in 1 BLISTER PACK", "package_ndc": "0904-7443-61", "marketing_start_date": "20251121"}], "brand_name": "Clonidine Hydrochloride", "product_id": "0904-7443_7edda115-1bfd-4d8c-a3cd-2c8492ba56cb", "dosage_form": "TABLET", "pharm_class": ["Adrenergic alpha2-Agonists [MoA]", "Central alpha-2 Adrenergic Agonist [EPC]"], "product_ndc": "0904-7443", "generic_name": "clonidine hydrochloride", "labeler_name": "Major Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Clonidine Hydrochloride", "active_ingredients": [{"name": "CLONIDINE HYDROCHLORIDE", "strength": ".2 mg/1"}], "application_number": "ANDA077901", "marketing_category": "ANDA", "marketing_start_date": "20251121", "listing_expiration_date": "20261231"}