clonidine hydrochloride

Generic: clonidine hydrochloride

Labeler: alembic pharmaceuticals limited
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name clonidine hydrochloride
Generic Name clonidine hydrochloride
Labeler alembic pharmaceuticals limited
Dosage Form TABLET
Routes
ORAL
Active Ingredients

clonidine hydrochloride .1 mg/1

Manufacturer
Alembic Pharmaceuticals Limited

Identifiers & Regulatory

Product NDC 46708-306
Product ID 46708-306_f2ae3ce9-d436-4616-a3eb-7838af98b9a6
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA091368
Listing Expiration 2026-12-31
Marketing Start 2016-05-03

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 46708306
Hyphenated Format 46708-306

Supplemental Identifiers

RxCUI
884173 884185 884189
UPC
0346708307301 0346708306304 0346708308308
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 ANDA091368 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • .1 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 CARTON (46708-306-10)
  • 30 TABLET in 1 BOTTLE (46708-306-30)
  • 100 TABLET in 1 BOTTLE (46708-306-31)
  • 500 TABLET in 1 BOTTLE (46708-306-71)
  • 1000 TABLET in 1 BOTTLE (46708-306-91)
source: ndc

Packages (5)

46708-306-10 100 TABLET in 1 CARTON (46708-306-10) 46708-306-30 30 TABLET in 1 BOTTLE (46708-306-30) 46708-306-31 100 TABLET in 1 BOTTLE (46708-306-31) 46708-306-71 500 TABLET in 1 BOTTLE (46708-306-71) 46708-306-91 1000 TABLET in 1 BOTTLE (46708-306-91)

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": "f2ae3ce9-d436-4616-a3eb-7838af98b9a6", "openfda": {"upc": ["0346708307301", "0346708306304", "0346708308308"], "unii": ["W76I6XXF06"], "rxcui": ["884173", "884185", "884189"], "spl_set_id": ["88a8db46-0fc9-48cd-b7cc-ac9c9cdea100"], "manufacturer_name": ["Alembic Pharmaceuticals Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 CARTON (46708-306-10)", "package_ndc": "46708-306-10", "marketing_start_date": "20160503"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (46708-306-30)", "package_ndc": "46708-306-30", "marketing_start_date": "20160503"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (46708-306-31)", "package_ndc": "46708-306-31", "marketing_start_date": "20160503"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (46708-306-71)", "package_ndc": "46708-306-71", "marketing_start_date": "20160503"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (46708-306-91)", "package_ndc": "46708-306-91", "marketing_start_date": "20160503"}], "brand_name": "clonidine hydrochloride", "product_id": "46708-306_f2ae3ce9-d436-4616-a3eb-7838af98b9a6", "dosage_form": "TABLET", "pharm_class": ["Adrenergic alpha2-Agonists [MoA]", "Central alpha-2 Adrenergic Agonist [EPC]"], "product_ndc": "46708-306", "generic_name": "Clonidine Hydrochloride", "labeler_name": "Alembic Pharmaceuticals Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "clonidine hydrochloride", "active_ingredients": [{"name": "CLONIDINE HYDROCHLORIDE", "strength": ".1 mg/1"}], "application_number": "ANDA091368", "marketing_category": "ANDA", "marketing_start_date": "20160503", "listing_expiration_date": "20261231"}