clonidine hydrochloride

Generic: clonidine hydrochloride

Labeler: a-s medication solutions
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name clonidine hydrochloride
Generic Name clonidine hydrochloride
Labeler a-s medication solutions
Dosage Form TABLET
Routes
ORAL
Active Ingredients

clonidine hydrochloride .1 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-6946
Product ID 50090-6946_fc7d3325-21d9-460a-a5a0-a5bfbdac9cdb
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA078895
Listing Expiration 2026-12-31
Marketing Start 2020-12-24

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 500906946
Hyphenated Format 50090-6946

Supplemental Identifiers

RxCUI
884173
UNII
W76I6XXF06

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 ANDA078895 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • .1 mg/1
source: ndc
Packaging
  • 90 TABLET in 1 BOTTLE (50090-6946-0)
source: ndc

Packages (1)

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": "fc7d3325-21d9-460a-a5a0-a5bfbdac9cdb", "openfda": {"unii": ["W76I6XXF06"], "rxcui": ["884173"], "spl_set_id": ["c5c85b76-4d5c-47f0-bafb-31efe1fbaed3"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (50090-6946-0)", "package_ndc": "50090-6946-0", "marketing_start_date": "20231218"}], "brand_name": "clonidine hydrochloride", "product_id": "50090-6946_fc7d3325-21d9-460a-a5a0-a5bfbdac9cdb", "dosage_form": "TABLET", "pharm_class": ["Adrenergic alpha2-Agonists [MoA]", "Central alpha-2 Adrenergic Agonist [EPC]"], "product_ndc": "50090-6946", "generic_name": "clonidine hydrochloride", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "clonidine hydrochloride", "active_ingredients": [{"name": "CLONIDINE HYDROCHLORIDE", "strength": ".1 mg/1"}], "application_number": "ANDA078895", "marketing_category": "ANDA", "marketing_start_date": "20201224", "listing_expiration_date": "20261231"}