clonidine hydrochloride

Generic: clonidine hydrochloride

Labeler: pd-rx pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name clonidine hydrochloride
Generic Name clonidine hydrochloride
Labeler pd-rx pharmaceuticals, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

clonidine hydrochloride .2 mg/1

Manufacturer
PD-Rx Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 43063-925
Product ID 43063-925_415e5e43-7ecc-06d8-e063-6294a90a132b
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA078895
Listing Expiration 2026-12-31
Marketing Start 2009-09-21

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 43063925
Hyphenated Format 43063-925

Supplemental Identifiers

RxCUI
884185
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
  • .2 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE, PLASTIC (43063-925-30)
source: ndc

Packages (1)

43063-925-30 30 TABLET in 1 BOTTLE, PLASTIC (43063-925-30)

Ingredients (1)

clonidine hydrochloride (.2 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": "415e5e43-7ecc-06d8-e063-6294a90a132b", "openfda": {"unii": ["W76I6XXF06"], "rxcui": ["884185"], "spl_set_id": ["ea1527a5-4939-4ff7-a827-f88a9113a07d"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (43063-925-30)", "package_ndc": "43063-925-30", "marketing_start_date": "20190107"}], "brand_name": "clonidine hydrochloride", "product_id": "43063-925_415e5e43-7ecc-06d8-e063-6294a90a132b", "dosage_form": "TABLET", "pharm_class": ["Adrenergic alpha2-Agonists [MoA]", "Central alpha-2 Adrenergic Agonist [EPC]"], "product_ndc": "43063-925", "generic_name": "clonidine hydrochloride", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "clonidine hydrochloride", "active_ingredients": [{"name": "CLONIDINE HYDROCHLORIDE", "strength": ".2 mg/1"}], "application_number": "ANDA078895", "marketing_category": "ANDA", "marketing_start_date": "20090921", "listing_expiration_date": "20261231"}