clonidine hydrochloride
Generic: clonidine hydrochloride
Labeler: major pharmaceuticalsDrug Facts
Product Profile
Brand Name
clonidine hydrochloride
Generic Name
clonidine hydrochloride
Labeler
major pharmaceuticals
Dosage Form
TABLET
Routes
Active Ingredients
clonidine hydrochloride .2 mg/1
Manufacturer
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
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
09047443
Hyphenated Format
0904-7443
Supplemental Identifiers
RxCUI
UNII
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
source: ndc
Resolved Composition
Strengths
- .2 mg/1
Packaging
- 100 BLISTER PACK in 1 CARTON (0904-7443-61) / 1 TABLET in 1 BLISTER PACK
Packages (1)
Ingredients (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"}