clonidine hydrochloride
Generic: clonidine hydrochloride
Labeler: actavis pharma, inc.Drug Facts
Product Profile
Brand Name
clonidine hydrochloride
Generic Name
clonidine hydrochloride
Labeler
actavis pharma, inc.
Dosage Form
TABLET
Routes
Active Ingredients
clonidine hydrochloride .2 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
0228-2128
Product ID
0228-2128_860129c9-0bba-471e-a90c-b6bede1833b8
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA070975
Listing Expiration
2026-12-31
Marketing Start
1995-01-03
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
02282128
Hyphenated Format
0228-2128
Supplemental Identifiers
RxCUI
UPC
UNII
Packaging Origin
Original Packager
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
ANDA070975 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- .2 mg/1
Packaging
- 100 TABLET in 1 BOTTLE (0228-2128-10)
- 500 TABLET in 1 BOTTLE (0228-2128-50)
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "860129c9-0bba-471e-a90c-b6bede1833b8", "openfda": {"upc": ["0302282128107", "0302282129104", "0302282127100"], "unii": ["W76I6XXF06"], "rxcui": ["884173", "884185", "884189"], "spl_set_id": ["a842ab83-3531-44dd-a8a8-64dd89e87026"], "manufacturer_name": ["Actavis Pharma, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (0228-2128-10)", "package_ndc": "0228-2128-10", "marketing_start_date": "19950103"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (0228-2128-50)", "package_ndc": "0228-2128-50", "marketing_start_date": "19950103"}], "brand_name": "Clonidine Hydrochloride", "product_id": "0228-2128_860129c9-0bba-471e-a90c-b6bede1833b8", "dosage_form": "TABLET", "pharm_class": ["Adrenergic alpha2-Agonists [MoA]", "Central alpha-2 Adrenergic Agonist [EPC]"], "product_ndc": "0228-2128", "generic_name": "Clonidine Hydrochloride", "labeler_name": "Actavis Pharma, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Clonidine Hydrochloride", "active_ingredients": [{"name": "CLONIDINE HYDROCHLORIDE", "strength": ".2 mg/1"}], "application_number": "ANDA070975", "marketing_category": "ANDA", "marketing_start_date": "19950103", "listing_expiration_date": "20261231"}