clonidine hydrochloride

Generic: clonidine hydrochloride

Labeler: solco healthcare llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name clonidine hydrochloride
Generic Name clonidine hydrochloride
Labeler solco healthcare llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

clonidine hydrochloride .1 mg/1

Manufacturer
Solco Healthcare LLC

Identifiers & Regulatory

Product NDC 43547-565
Product ID 43547-565_d09551ff-dfac-4525-8122-97b4463e98ea
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA077901
Listing Expiration 2026-12-31
Marketing Start 2023-01-05

Pharmacologic Class

Classes
adrenergic alpha2-agonists [moa] central alpha-2 adrenergic agonist [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 43547565
Hyphenated Format 43547-565

Supplemental Identifiers

RxCUI
884173 884185 884189
UPC
0343547567101 0343547565107 0343547566104
UNII
W76I6XXF06

Packaging Origin

Original Packager
true

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
ORAL
source: ndc

Resolved Composition

Strengths
  • .1 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE, PLASTIC (43547-565-10)
  • 1000 TABLET in 1 BOTTLE, PLASTIC (43547-565-11)
source: ndc

Packages (2)

Ingredients (1)

clonidine hydrochloride (.1 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "d09551ff-dfac-4525-8122-97b4463e98ea", "openfda": {"upc": ["0343547567101", "0343547565107", "0343547566104"], "unii": ["W76I6XXF06"], "rxcui": ["884173", "884185", "884189"], "spl_set_id": ["2bbfea75-9241-4c3a-84f5-342ccb3cdf16"], "manufacturer_name": ["Solco Healthcare LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (43547-565-10)", "package_ndc": "43547-565-10", "marketing_start_date": "20230105"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE, PLASTIC (43547-565-11)", "package_ndc": "43547-565-11", "marketing_start_date": "20230105"}], "brand_name": "Clonidine Hydrochloride", "product_id": "43547-565_d09551ff-dfac-4525-8122-97b4463e98ea", "dosage_form": "TABLET", "pharm_class": ["Adrenergic alpha2-Agonists [MoA]", "Central alpha-2 Adrenergic Agonist [EPC]"], "product_ndc": "43547-565", "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": "ANDA077901", "marketing_category": "ANDA", "marketing_start_date": "20230105", "listing_expiration_date": "20261231"}