clonidine hydrochloride
Generic: clonidine hydrochloride
Labeler: bluepoint laboratoriesDrug Facts
Product Profile
Brand Name
clonidine hydrochloride
Generic Name
clonidine hydrochloride
Labeler
bluepoint laboratories
Dosage Form
TABLET
Routes
Active Ingredients
clonidine hydrochloride .2 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
68001-238
Product ID
68001-238_42c4b1f4-a2c5-e21f-e063-6294a90aa481
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
68001238
Hyphenated Format
68001-238
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 (68001-238-00)
- 500 TABLET in 1 BOTTLE (68001-238-03)
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "42c4b1f4-a2c5-e21f-e063-6294a90aa481", "openfda": {"upc": ["0368001239004", "0368001238007", "0368001237000"], "unii": ["W76I6XXF06"], "rxcui": ["884173", "884185", "884189"], "spl_set_id": ["1ea412db-d847-4094-be83-e3bd7328537a"], "manufacturer_name": ["BluePoint Laboratories"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (68001-238-00)", "package_ndc": "68001-238-00", "marketing_start_date": "19950103"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (68001-238-03)", "package_ndc": "68001-238-03", "marketing_start_date": "19950103"}], "brand_name": "Clonidine Hydrochloride", "product_id": "68001-238_42c4b1f4-a2c5-e21f-e063-6294a90aa481", "dosage_form": "TABLET", "pharm_class": ["Adrenergic alpha2-Agonists [MoA]", "Central alpha-2 Adrenergic Agonist [EPC]"], "product_ndc": "68001-238", "generic_name": "Clonidine Hydrochloride", "labeler_name": "BluePoint Laboratories", "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"}