clonidine hydrochloride

Generic: clonidine hydrochloride

Labeler: remedyrepack inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name clonidine hydrochloride
Generic Name clonidine hydrochloride
Labeler remedyrepack inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

clonidine hydrochloride .1 mg/1

Manufacturer
REMEDYREPACK INC.

Identifiers & Regulatory

Product NDC 70518-3162
Product ID 70518-3162_49d7621e-7c44-a511-e063-6394a90a614a
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA078895
Listing Expiration 2027-12-31
Marketing Start 2021-07-19

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 705183162
Hyphenated Format 70518-3162

Supplemental Identifiers

RxCUI
884173
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
  • 30 TABLET in 1 BLISTER PACK (70518-3162-1)
  • 180 TABLET in 1 BOTTLE, PLASTIC (70518-3162-4)
  • 90 TABLET in 1 BOTTLE, PLASTIC (70518-3162-5)
  • 180 TABLET in 1 BOTTLE, PLASTIC (70518-3162-6)
  • 30 TABLET in 1 BOTTLE, PLASTIC (70518-3162-7)
source: ndc

Packages (5)

70518-3162-1 30 TABLET in 1 BLISTER PACK (70518-3162-1) 70518-3162-4 180 TABLET in 1 BOTTLE, PLASTIC (70518-3162-4) 70518-3162-5 90 TABLET in 1 BOTTLE, PLASTIC (70518-3162-5) 70518-3162-6 180 TABLET in 1 BOTTLE, PLASTIC (70518-3162-6) 70518-3162-7 30 TABLET in 1 BOTTLE, PLASTIC (70518-3162-7)

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": "49d7621e-7c44-a511-e063-6394a90a614a", "openfda": {"unii": ["W76I6XXF06"], "rxcui": ["884173"], "spl_set_id": ["e5d24f52-e0c2-428d-b647-481d63ffd95f"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (70518-3162-1)", "package_ndc": "70518-3162-1", "marketing_start_date": "20230227"}, {"sample": false, "description": "180 TABLET in 1 BOTTLE, PLASTIC (70518-3162-4)", "package_ndc": "70518-3162-4", "marketing_start_date": "20241015"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (70518-3162-5)", "package_ndc": "70518-3162-5", "marketing_start_date": "20250912"}, {"sample": false, "description": "180 TABLET in 1 BOTTLE, PLASTIC (70518-3162-6)", "package_ndc": "70518-3162-6", "marketing_start_date": "20251031"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (70518-3162-7)", "package_ndc": "70518-3162-7", "marketing_start_date": "20260201"}], "brand_name": "clonidine hydrochloride", "product_id": "70518-3162_49d7621e-7c44-a511-e063-6394a90a614a", "dosage_form": "TABLET", "pharm_class": ["Adrenergic alpha2-Agonists [MoA]", "Central alpha-2 Adrenergic Agonist [EPC]"], "product_ndc": "70518-3162", "generic_name": "clonidine hydrochloride", "labeler_name": "REMEDYREPACK 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": "20210719", "listing_expiration_date": "20271231"}