clonidine hydrochloride
Generic: clonidine hydrochloride
Labeler: remedyrepack inc.Drug Facts
Product Profile
Brand Name
clonidine hydrochloride
Generic Name
clonidine hydrochloride
Labeler
remedyrepack inc.
Dosage Form
TABLET
Routes
Active Ingredients
clonidine hydrochloride .1 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
70518-4342
Product ID
70518-4342_35bb250a-9f02-c3dc-e063-6394a90a87e7
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA070974
Listing Expiration
2026-12-31
Marketing Start
2025-05-18
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
705184342
Hyphenated Format
70518-4342
Supplemental Identifiers
RxCUI
UNII
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
ANDA070974 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- .1 mg/1
Packaging
- 30 TABLET in 1 BOTTLE, PLASTIC (70518-4342-0)
- 30 TABLET in 1 BLISTER PACK (70518-4342-1)
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "35bb250a-9f02-c3dc-e063-6394a90a87e7", "openfda": {"unii": ["W76I6XXF06"], "rxcui": ["884173"], "spl_set_id": ["00c6d67a-bb11-4884-9eeb-4e1b8701a08b"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (70518-4342-0)", "package_ndc": "70518-4342-0", "marketing_start_date": "20250518"}, {"sample": false, "description": "30 TABLET in 1 BLISTER PACK (70518-4342-1)", "package_ndc": "70518-4342-1", "marketing_start_date": "20250519"}], "brand_name": "Clonidine Hydrochloride", "product_id": "70518-4342_35bb250a-9f02-c3dc-e063-6394a90a87e7", "dosage_form": "TABLET", "pharm_class": ["Adrenergic alpha2-Agonists [MoA]", "Central alpha-2 Adrenergic Agonist [EPC]"], "product_ndc": "70518-4342", "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": "ANDA070974", "marketing_category": "ANDA", "marketing_start_date": "20250518", "listing_expiration_date": "20261231"}