clonidine hydrochloride

Generic: clonidine hydrochloride

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

Drug Facts

Product Profile

Brand Name clonidine hydrochloride
Generic Name clonidine hydrochloride
Labeler verityrx, llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

clonidine hydrochloride .1 mg/1

Manufacturer
VERITYRX, LLC

Identifiers & Regulatory

Product NDC 83939-0006
Product ID 83939-0006_427939a4-6bc0-0d80-e063-6294a90aa2a0
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 839390006
Hyphenated Format 83939-0006

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
  • 1 TABLET in 1 POUCH (83939-0006-1)
  • 50 POUCH in 1 BOX, UNIT-DOSE (83939-0006-2) / 1 TABLET in 1 POUCH
  • 100 POUCH in 1 BOX, UNIT-DOSE (83939-0006-3) / 1 TABLET in 1 POUCH
source: ndc

Packages (3)

83939-0006-1 1 TABLET in 1 POUCH (83939-0006-1) 83939-0006-2 50 POUCH in 1 BOX, UNIT-DOSE (83939-0006-2) / 1 TABLET in 1 POUCH 83939-0006-3 100 POUCH in 1 BOX, UNIT-DOSE (83939-0006-3) / 1 TABLET in 1 POUCH

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": "427939a4-6bc0-0d80-e063-6294a90aa2a0", "openfda": {"unii": ["W76I6XXF06"], "rxcui": ["884173"], "spl_set_id": ["427939a4-6bbf-0d80-e063-6294a90aa2a0"], "manufacturer_name": ["VERITYRX, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "1 TABLET in 1 POUCH (83939-0006-1)", "package_ndc": "83939-0006-1", "marketing_start_date": "20251103"}, {"sample": false, "description": "50 POUCH in 1 BOX, UNIT-DOSE (83939-0006-2)  / 1 TABLET in 1 POUCH", "package_ndc": "83939-0006-2", "marketing_start_date": "20251103"}, {"sample": false, "description": "100 POUCH in 1 BOX, UNIT-DOSE (83939-0006-3)  / 1 TABLET in 1 POUCH", "package_ndc": "83939-0006-3", "marketing_start_date": "20251103"}], "brand_name": "clonidine hydrochloride", "product_id": "83939-0006_427939a4-6bc0-0d80-e063-6294a90aa2a0", "dosage_form": "TABLET", "pharm_class": ["Adrenergic alpha2-Agonists [MoA]", "Central alpha-2 Adrenergic Agonist [EPC]"], "product_ndc": "83939-0006", "generic_name": "clonidine hydrochloride", "labeler_name": "VERITYRX, LLC", "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"}