clonidine hydrochloride
Generic: clonidine hydrochloride
Labeler: a-s medication solutionsDrug Facts
Product Profile
Brand Name
clonidine hydrochloride
Generic Name
clonidine hydrochloride
Labeler
a-s medication solutions
Dosage Form
TABLET
Routes
Active Ingredients
clonidine hydrochloride .3 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
50090-1910
Product ID
50090-1910_a1e2050a-9fa4-4553-b069-5e83ec86bdb5
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA078895
Listing Expiration
2026-12-31
Marketing Start
2009-09-21
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
500901910
Hyphenated Format
50090-1910
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
ANDA078895 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- .3 mg/1
Packaging
- 100 TABLET in 1 BOTTLE (50090-1910-0)
- 60 TABLET in 1 BOTTLE (50090-1910-1)
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "a1e2050a-9fa4-4553-b069-5e83ec86bdb5", "openfda": {"unii": ["W76I6XXF06"], "rxcui": ["884173", "884185", "884189"], "spl_set_id": ["70c0c9f4-075d-4621-ae13-e8f03d814d5f"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (50090-1910-0)", "package_ndc": "50090-1910-0", "marketing_start_date": "20181101"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (50090-1910-1)", "package_ndc": "50090-1910-1", "marketing_start_date": "20150629"}], "brand_name": "clonidine hydrochloride", "product_id": "50090-1910_a1e2050a-9fa4-4553-b069-5e83ec86bdb5", "dosage_form": "TABLET", "pharm_class": ["Adrenergic alpha2-Agonists [MoA]", "Central alpha-2 Adrenergic Agonist [EPC]"], "product_ndc": "50090-1910", "generic_name": "clonidine hydrochloride", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "clonidine hydrochloride", "active_ingredients": [{"name": "CLONIDINE HYDROCHLORIDE", "strength": ".3 mg/1"}], "application_number": "ANDA078895", "marketing_category": "ANDA", "marketing_start_date": "20090921", "listing_expiration_date": "20261231"}