clonidine hydrochloride
Generic: clonidine hydrochloride
Labeler: bryant ranch prepackDrug Facts
Product Profile
Brand Name
clonidine hydrochloride
Generic Name
clonidine hydrochloride
Labeler
bryant ranch prepack
Dosage Form
TABLET
Routes
Active Ingredients
clonidine hydrochloride .3 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
71335-2889
Product ID
71335-2889_42540d3c-5254-6bc7-e063-6294a90adf98
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA202297
Listing Expiration
2026-12-31
Marketing Start
2020-07-01
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
713352889
Hyphenated Format
71335-2889
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
- .3 mg/1
Packaging
- 500 TABLET in 1 BOTTLE (71335-2889-1)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "42540d3c-5254-6bc7-e063-6294a90adf98", "openfda": {"unii": ["W76I6XXF06"], "rxcui": ["884189"], "spl_set_id": ["60171b1d-03af-4849-a030-6260192b11ce"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET in 1 BOTTLE (71335-2889-1)", "package_ndc": "71335-2889-1", "marketing_start_date": "20251029"}], "brand_name": "Clonidine Hydrochloride", "product_id": "71335-2889_42540d3c-5254-6bc7-e063-6294a90adf98", "dosage_form": "TABLET", "pharm_class": ["Adrenergic alpha2-Agonists [MoA]", "Central alpha-2 Adrenergic Agonist [EPC]"], "product_ndc": "71335-2889", "generic_name": "Clonidine Hydrochloride", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Clonidine Hydrochloride", "active_ingredients": [{"name": "CLONIDINE HYDROCHLORIDE", "strength": ".3 mg/1"}], "application_number": "ANDA202297", "marketing_category": "ANDA", "marketing_start_date": "20200701", "listing_expiration_date": "20261231"}