clonidine hydrochloride

Generic: clonidine hydrochloride

Labeler: xiamen lp pharmaceutical co., ltd.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name clonidine hydrochloride
Generic Name clonidine hydrochloride
Labeler xiamen lp pharmaceutical co., ltd.
Dosage Form TABLET, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

clonidine hydrochloride .1 mg/1

Manufacturer
Xiamen LP Pharmaceutical Co., Ltd.

Identifiers & Regulatory

Product NDC 71034-001
Product ID 71034-001_b2b1f979-6a18-ad41-e053-2995a90ad14a
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA209757
Listing Expiration 2026-12-31
Marketing Start 2017-12-01

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 71034001
Hyphenated Format 71034-001

Supplemental Identifiers

RxCUI
1013930
UPC
0371034001609
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 ANDA209757 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • .1 mg/1
source: ndc
Packaging
  • 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71034-001-60)
source: ndc

Packages (1)

71034-001-60 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71034-001-60)

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": "b2b1f979-6a18-ad41-e053-2995a90ad14a", "openfda": {"upc": ["0371034001609"], "unii": ["W76I6XXF06"], "rxcui": ["1013930"], "spl_set_id": ["7676af27-4d8f-49c4-a50f-6b0892e73c8f"], "manufacturer_name": ["Xiamen LP Pharmaceutical Co., Ltd."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71034-001-60)", "package_ndc": "71034-001-60", "marketing_start_date": "20171201"}], "brand_name": "Clonidine Hydrochloride", "product_id": "71034-001_b2b1f979-6a18-ad41-e053-2995a90ad14a", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Adrenergic alpha2-Agonists [MoA]", "Central alpha-2 Adrenergic Agonist [EPC]"], "product_ndc": "71034-001", "generic_name": "Clonidine Hydrochloride", "labeler_name": "Xiamen LP Pharmaceutical Co., Ltd.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Clonidine Hydrochloride", "active_ingredients": [{"name": "CLONIDINE HYDROCHLORIDE", "strength": ".1 mg/1"}], "application_number": "ANDA209757", "marketing_category": "ANDA", "marketing_start_date": "20171201", "listing_expiration_date": "20261231"}