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 .1 mg/1

Manufacturer
PD-Rx Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 43063-817
Product ID 43063-817_415b969a-7fa4-b1dc-e063-6294a90ae971
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 43063817
Hyphenated Format 43063-817

Supplemental Identifiers

RxCUI
884173
UPC
0343063817087
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
  • 8 TABLET in 1 BOTTLE, PLASTIC (43063-817-08)
  • 15 TABLET in 1 BOTTLE, PLASTIC (43063-817-15)
  • 30 TABLET in 1 BOTTLE, PLASTIC (43063-817-30)
  • 60 TABLET in 1 BOTTLE, PLASTIC (43063-817-60)
source: ndc

Packages (4)

43063-817-08 8 TABLET in 1 BOTTLE, PLASTIC (43063-817-08) 43063-817-15 15 TABLET in 1 BOTTLE, PLASTIC (43063-817-15) 43063-817-30 30 TABLET in 1 BOTTLE, PLASTIC (43063-817-30) 43063-817-60 60 TABLET in 1 BOTTLE, PLASTIC (43063-817-60)

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": "415b969a-7fa4-b1dc-e063-6294a90ae971", "openfda": {"upc": ["0343063817087"], "unii": ["W76I6XXF06"], "rxcui": ["884173"], "spl_set_id": ["51a275e0-e998-4d92-9f37-d5ba9ff8190c"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "8 TABLET in 1 BOTTLE, PLASTIC (43063-817-08)", "package_ndc": "43063-817-08", "marketing_start_date": "20190104"}, {"sample": false, "description": "15 TABLET in 1 BOTTLE, PLASTIC (43063-817-15)", "package_ndc": "43063-817-15", "marketing_start_date": "20190424"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (43063-817-30)", "package_ndc": "43063-817-30", "marketing_start_date": "20171218"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE, PLASTIC (43063-817-60)", "package_ndc": "43063-817-60", "marketing_start_date": "20171218"}], "brand_name": "clonidine hydrochloride", "product_id": "43063-817_415b969a-7fa4-b1dc-e063-6294a90ae971", "dosage_form": "TABLET", "pharm_class": ["Adrenergic alpha2-Agonists [MoA]", "Central alpha-2 Adrenergic Agonist [EPC]"], "product_ndc": "43063-817", "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": ".1 mg/1"}], "application_number": "ANDA078895", "marketing_category": "ANDA", "marketing_start_date": "20090921", "listing_expiration_date": "20261231"}