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 .2 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
70518-3295
Product ID
70518-3295_38dd1489-8625-2e37-e063-6394a90a00ee
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA202297
Listing Expiration
2026-12-31
Marketing Start
2021-12-14
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
705183295
Hyphenated Format
70518-3295
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
ANDA202297 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- .2 mg/1
Packaging
- 30 TABLET in 1 BLISTER PACK (70518-3295-0)
- 180 TABLET in 1 BOTTLE, PLASTIC (70518-3295-1)
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "38dd1489-8625-2e37-e063-6394a90a00ee", "openfda": {"unii": ["W76I6XXF06"], "rxcui": ["884185"], "spl_set_id": ["e413efdf-980b-4b33-80f1-5be899a10f01"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (70518-3295-0)", "package_ndc": "70518-3295-0", "marketing_start_date": "20211214"}, {"sample": false, "description": "180 TABLET in 1 BOTTLE, PLASTIC (70518-3295-1)", "package_ndc": "70518-3295-1", "marketing_start_date": "20250630"}], "brand_name": "Clonidine Hydrochloride", "product_id": "70518-3295_38dd1489-8625-2e37-e063-6394a90a00ee", "dosage_form": "TABLET", "pharm_class": ["Adrenergic alpha2-Agonists [MoA]", "Central alpha-2 Adrenergic Agonist [EPC]"], "product_ndc": "70518-3295", "generic_name": "Clonidine Hydrochloride", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Clonidine Hydrochloride", "active_ingredients": [{"name": "CLONIDINE HYDROCHLORIDE", "strength": ".2 mg/1"}], "application_number": "ANDA202297", "marketing_category": "ANDA", "marketing_start_date": "20211214", "listing_expiration_date": "20261231"}