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 50090-6744
Product ID 50090-6744_cce6ef3b-e6ae-44e3-9ff1-3e6314e148c0
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA070886
Listing Expiration 2026-12-31
Marketing Start 2021-06-02

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 500906744
Hyphenated Format 50090-6744

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 ANDA070886 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • .1 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (50090-6744-0)
  • 60 TABLET in 1 BOTTLE (50090-6744-1)
  • 100 TABLET in 1 BOTTLE (50090-6744-2)
  • 90 TABLET in 1 BOTTLE (50090-6744-7)
  • 180 TABLET in 1 BOTTLE (50090-6744-8)
source: ndc

Packages (5)

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": "cce6ef3b-e6ae-44e3-9ff1-3e6314e148c0", "openfda": {"unii": ["W76I6XXF06"], "rxcui": ["884173"], "spl_set_id": ["c7f473df-94ab-41db-8cc7-9a159d5e6dc4"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (50090-6744-0)", "package_ndc": "50090-6744-0", "marketing_start_date": "20231016"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (50090-6744-1)", "package_ndc": "50090-6744-1", "marketing_start_date": "20231016"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (50090-6744-2)", "package_ndc": "50090-6744-2", "marketing_start_date": "20231016"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (50090-6744-7)", "package_ndc": "50090-6744-7", "marketing_start_date": "20231016"}, {"sample": false, "description": "180 TABLET in 1 BOTTLE (50090-6744-8)", "package_ndc": "50090-6744-8", "marketing_start_date": "20231016"}], "brand_name": "Clonidine Hydrochloride", "product_id": "50090-6744_cce6ef3b-e6ae-44e3-9ff1-3e6314e148c0", "dosage_form": "TABLET", "pharm_class": ["Adrenergic alpha2-Agonists [MoA]", "Central alpha-2 Adrenergic Agonist [EPC]"], "product_ndc": "50090-6744", "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": "ANDA070886", "marketing_category": "ANDA", "marketing_start_date": "20210602", "listing_expiration_date": "20261231"}