clonidine hydrochloride

Generic: clonidine hydrochloride

Labeler: lupin pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name clonidine hydrochloride
Generic Name clonidine hydrochloride
Labeler lupin pharmaceuticals, inc.
Dosage Form TABLET, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

clonidine hydrochloride .1 mg/1

Manufacturer
Lupin Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 68180-606
Product ID 68180-606_deb39225-24ce-45aa-a32b-bfa70bb8d25b
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA209285
Listing Expiration 2026-12-31
Marketing Start 2018-02-07

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 68180606
Hyphenated Format 68180-606

Supplemental Identifiers

RxCUI
1013930
UPC
0368180606093 0368180606062 0368180606079
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 ANDA209285 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • .1 mg/1
source: ndc
Packaging
  • 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (68180-606-07)
source: ndc

Packages (1)

68180-606-07 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (68180-606-07)

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": "deb39225-24ce-45aa-a32b-bfa70bb8d25b", "openfda": {"upc": ["0368180606093", "0368180606062", "0368180606079"], "unii": ["W76I6XXF06"], "rxcui": ["1013930"], "spl_set_id": ["745c8731-63e0-47ce-96d3-6a4d21c655e2"], "manufacturer_name": ["Lupin Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, EXTENDED RELEASE in 1 BOTTLE (68180-606-07)", "package_ndc": "68180-606-07", "marketing_start_date": "20180207"}], "brand_name": "Clonidine Hydrochloride", "product_id": "68180-606_deb39225-24ce-45aa-a32b-bfa70bb8d25b", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Adrenergic alpha2-Agonists [MoA]", "Central alpha-2 Adrenergic Agonist [EPC]"], "product_ndc": "68180-606", "generic_name": "Clonidine Hydrochloride", "labeler_name": "Lupin Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Clonidine Hydrochloride", "active_ingredients": [{"name": "CLONIDINE HYDROCHLORIDE", "strength": ".1 mg/1"}], "application_number": "ANDA209285", "marketing_category": "ANDA", "marketing_start_date": "20180207", "listing_expiration_date": "20261231"}