clonidine

Generic: clonidine

Labeler: ingenus pharmaceuticals, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name clonidine
Generic Name clonidine
Labeler ingenus pharmaceuticals, llc
Dosage Form TABLET, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

clonidine hydrochloride .1 mg/1

Manufacturer
Ingenus Pharmaceuticals, LLC

Identifiers & Regulatory

Product NDC 50742-247
Product ID 50742-247_4f2ad773-518b-4532-bb69-8ff28c4f24c4
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA209675
Listing Expiration 2026-12-31
Marketing Start 2019-03-05

Pharmacologic Class

Classes
adrenergic alpha2-agonists [moa] central alpha-2 adrenergic agonist [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 50742247
Hyphenated Format 50742-247

Supplemental Identifiers

RxCUI
1013930
UPC
0350742247608
UNII
W76I6XXF06

Packaging Origin

Original Packager
true

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 (source: ndc)
Generic Name clonidine (source: ndc)
Application Number ANDA209675 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • .1 mg/1
source: ndc
Packaging
  • 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (50742-247-05)
  • 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (50742-247-30)
  • 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (50742-247-60)
source: ndc

Packages (3)

50742-247-05 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (50742-247-05) 50742-247-30 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (50742-247-30) 50742-247-60 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (50742-247-60)

Ingredients (1)

clonidine hydrochloride (.1 mg/1)

Linked Drug Pages (1)

Clonidine ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "4f2ad773-518b-4532-bb69-8ff28c4f24c4", "openfda": {"upc": ["0350742247608"], "unii": ["W76I6XXF06"], "rxcui": ["1013930"], "spl_set_id": ["99485427-a120-4fc7-bb61-25857d1900ec"], "manufacturer_name": ["Ingenus Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET, EXTENDED RELEASE in 1 BOTTLE (50742-247-05)", "package_ndc": "50742-247-05", "marketing_start_date": "20190305"}, {"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (50742-247-30)", "package_ndc": "50742-247-30", "marketing_start_date": "20190305"}, {"sample": false, "description": "60 TABLET, EXTENDED RELEASE in 1 BOTTLE (50742-247-60)", "package_ndc": "50742-247-60", "marketing_start_date": "20190305"}], "brand_name": "Clonidine", "product_id": "50742-247_4f2ad773-518b-4532-bb69-8ff28c4f24c4", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Adrenergic alpha2-Agonists [MoA]", "Central alpha-2 Adrenergic Agonist [EPC]"], "product_ndc": "50742-247", "generic_name": "clonidine", "labeler_name": "Ingenus Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Clonidine", "active_ingredients": [{"name": "CLONIDINE HYDROCHLORIDE", "strength": ".1 mg/1"}], "application_number": "ANDA209675", "marketing_category": "ANDA", "marketing_start_date": "20190305", "listing_expiration_date": "20261231"}