clonidine hydrochloride
Generic: clonidine hydrochloride
Labeler: unichem pharmaceuticals (usa), inc.Drug Facts
Product Profile
Brand Name
clonidine hydrochloride
Generic Name
clonidine hydrochloride
Labeler
unichem pharmaceuticals (usa), inc.
Dosage Form
TABLET
Routes
Active Ingredients
clonidine hydrochloride .1 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
29300-135
Product ID
29300-135_5929c96f-9fa9-4399-84aa-28584da9966a
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
29300135
Hyphenated Format
29300-135
Supplemental Identifiers
RxCUI
UPC
UNII
Packaging Origin
Original Packager
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
- .1 mg/1
Packaging
- 100 TABLET in 1 BOTTLE, PLASTIC (29300-135-01)
- 500 TABLET in 1 BOTTLE, PLASTIC (29300-135-05)
- 1000 TABLET in 1 BOTTLE, PLASTIC (29300-135-10)
- 5000 TABLET in 1 BOTTLE, PLASTIC (29300-135-50)
Packages (4)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "5929c96f-9fa9-4399-84aa-28584da9966a", "openfda": {"upc": ["0329300136012", "0329300135015", "0329300468014", "0329300137019"], "unii": ["W76I6XXF06"], "rxcui": ["884173", "884185", "884189"], "spl_set_id": ["21bfa28f-20df-43fd-bb80-b720d3b40696"], "manufacturer_name": ["Unichem Pharmaceuticals (USA), Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (29300-135-01)", "package_ndc": "29300-135-01", "marketing_start_date": "20090921"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE, PLASTIC (29300-135-05)", "package_ndc": "29300-135-05", "marketing_start_date": "20090921"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE, PLASTIC (29300-135-10)", "package_ndc": "29300-135-10", "marketing_start_date": "20090921"}, {"sample": false, "description": "5000 TABLET in 1 BOTTLE, PLASTIC (29300-135-50)", "package_ndc": "29300-135-50", "marketing_start_date": "20090921"}], "brand_name": "clonidine hydrochloride", "product_id": "29300-135_5929c96f-9fa9-4399-84aa-28584da9966a", "dosage_form": "TABLET", "pharm_class": ["Adrenergic alpha2-Agonists [MoA]", "Central alpha-2 Adrenergic Agonist [EPC]"], "product_ndc": "29300-135", "generic_name": "clonidine hydrochloride", "labeler_name": "Unichem Pharmaceuticals (USA), 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": "20090921", "listing_expiration_date": "20261231"}