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, EXTENDED RELEASE
Routes
Active Ingredients
clonidine hydrochloride .1 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
68001-568
Product ID
68001-568_3c4f16d2-af44-ddf6-e063-6294a90aae36
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA209686
Listing Expiration
2026-12-31
Marketing Start
2023-08-24
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
68001568
Hyphenated Format
68001-568
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
ANDA209686 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- .1 mg/1
Packaging
- 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (68001-568-06)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3c4f16d2-af44-ddf6-e063-6294a90aae36", "openfda": {"upc": ["0368001568067"], "unii": ["W76I6XXF06"], "rxcui": ["1013930"], "spl_set_id": ["f34ae077-4ace-4e0a-bc87-d559b1c5bf2f"], "manufacturer_name": ["BluePoint Laboratories"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, EXTENDED RELEASE in 1 BOTTLE (68001-568-06)", "package_ndc": "68001-568-06", "marketing_start_date": "20230824"}], "brand_name": "Clonidine hydrochloride", "product_id": "68001-568_3c4f16d2-af44-ddf6-e063-6294a90aae36", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Adrenergic alpha2-Agonists [MoA]", "Central alpha-2 Adrenergic Agonist [EPC]"], "product_ndc": "68001-568", "generic_name": "Clonidine hydrochloride", "labeler_name": "BluePoint Laboratories", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Clonidine hydrochloride", "active_ingredients": [{"name": "CLONIDINE HYDROCHLORIDE", "strength": ".1 mg/1"}], "application_number": "ANDA209686", "marketing_category": "ANDA", "marketing_start_date": "20230824", "listing_expiration_date": "20261231"}