clonidine hydrochloride

Generic: clonidine hydrochloride

Labeler: somerset therapeutics, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name clonidine hydrochloride
Generic Name clonidine hydrochloride
Labeler somerset therapeutics, llc
Dosage Form TABLET, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

clonidine hydrochloride .1 mg/1

Manufacturer
Somerset Therapeutics, LLC

Identifiers & Regulatory

Product NDC 70069-044
Product ID 70069-044_b1e7ffe5-7d5f-4e02-a9c9-3d9ad3fac23e
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA211433
Listing Expiration 2026-12-31
Marketing Start 2025-03-04

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 70069044
Hyphenated Format 70069-044

Supplemental Identifiers

RxCUI
1013930
UPC
0370069044018
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 ANDA211433 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • .1 mg/1
source: ndc
Packaging
  • 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (70069-044-01)
source: ndc

Packages (1)

70069-044-01 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (70069-044-01)

Ingredients (1)

clonidine hydrochloride (.1 mg/1)

Linked Drug Pages (1)

Clonidine Hydrochloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "b1e7ffe5-7d5f-4e02-a9c9-3d9ad3fac23e", "openfda": {"upc": ["0370069044018"], "unii": ["W76I6XXF06"], "rxcui": ["1013930"], "spl_set_id": ["1b4fb182-8194-4fdd-bf9b-f7e60e734179"], "manufacturer_name": ["Somerset Therapeutics, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, EXTENDED RELEASE in 1 BOTTLE (70069-044-01)", "package_ndc": "70069-044-01", "marketing_start_date": "20250304"}], "brand_name": "Clonidine Hydrochloride", "product_id": "70069-044_b1e7ffe5-7d5f-4e02-a9c9-3d9ad3fac23e", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Adrenergic alpha2-Agonists [MoA]", "Central alpha-2 Adrenergic Agonist [EPC]"], "product_ndc": "70069-044", "generic_name": "Clonidine Hydrochloride", "labeler_name": "Somerset Therapeutics, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Clonidine Hydrochloride", "active_ingredients": [{"name": "CLONIDINE HYDROCHLORIDE", "strength": ".1 mg/1"}], "application_number": "ANDA211433", "marketing_category": "ANDA", "marketing_start_date": "20250304", "listing_expiration_date": "20261231"}