clonidine hydrochloride
Generic: clonidine hydrochloride
Labeler: solco healthcare llcDrug Facts
Product Profile
Brand Name
clonidine hydrochloride
Generic Name
clonidine hydrochloride
Labeler
solco healthcare llc
Dosage Form
TABLET, EXTENDED RELEASE
Routes
Active Ingredients
clonidine hydrochloride .1 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
43547-435
Product ID
43547-435_7fb6aea0-5714-48f7-9d60-c2e214755977
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA209757
Listing Expiration
2026-12-31
Marketing Start
2018-02-15
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
43547435
Hyphenated Format
43547-435
Supplemental Identifiers
RxCUI
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
ANDA209757 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- .1 mg/1
Packaging
- 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (43547-435-06)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "7fb6aea0-5714-48f7-9d60-c2e214755977", "openfda": {"unii": ["W76I6XXF06"], "rxcui": ["1013930"], "spl_set_id": ["03a53175-d301-4001-b28b-78ecd763c4ae"], "manufacturer_name": ["Solco Healthcare LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, EXTENDED RELEASE in 1 BOTTLE (43547-435-06)", "package_ndc": "43547-435-06", "marketing_start_date": "20180215"}], "brand_name": "Clonidine Hydrochloride", "product_id": "43547-435_7fb6aea0-5714-48f7-9d60-c2e214755977", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Adrenergic alpha2-Agonists [MoA]", "Central alpha-2 Adrenergic Agonist [EPC]"], "product_ndc": "43547-435", "generic_name": "Clonidine Hydrochloride", "labeler_name": "Solco Healthcare LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Clonidine Hydrochloride", "active_ingredients": [{"name": "CLONIDINE HYDROCHLORIDE", "strength": ".1 mg/1"}], "application_number": "ANDA209757", "marketing_category": "ANDA", "marketing_start_date": "20180215", "listing_expiration_date": "20261231"}