ropinirole

Generic: ropinirole

Labeler: direct rx
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name ropinirole
Generic Name ropinirole
Labeler direct rx
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

ropinirole hydrochloride 1 mg/1

Manufacturer
DIRECT RX

Identifiers & Regulatory

Product NDC 72189-222
Product ID 72189-222_2c28281e-fe37-b7e4-e063-6294a90ad4f7
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA204022
Listing Expiration 2026-12-31
Marketing Start 2021-05-20

Pharmacologic Class

Classes
dopamine agonists [moa] nonergot dopamine agonist [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72189222
Hyphenated Format 72189-222

Supplemental Identifiers

RxCUI
314208
UNII
D7ZD41RZI9

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 ropinirole (source: ndc)
Generic Name ropinirole (source: ndc)
Application Number ANDA204022 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1 mg/1
source: ndc
Packaging
  • 30 TABLET, FILM COATED in 1 BOTTLE (72189-222-30)
  • 60 TABLET, FILM COATED in 1 BOTTLE (72189-222-60)
source: ndc

Packages (2)

72189-222-30 30 TABLET, FILM COATED in 1 BOTTLE (72189-222-30) 72189-222-60 60 TABLET, FILM COATED in 1 BOTTLE (72189-222-60)

Ingredients (1)

ropinirole hydrochloride (1 mg/1)

Linked Drug Pages (1)

ROPINIROLE ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "2c28281e-fe37-b7e4-e063-6294a90ad4f7", "openfda": {"unii": ["D7ZD41RZI9"], "rxcui": ["314208"], "spl_set_id": ["c2c38b4c-b139-45f2-e053-2995a90a262c"], "manufacturer_name": ["DIRECT RX"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (72189-222-30)", "package_ndc": "72189-222-30", "marketing_start_date": "20210520"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (72189-222-60)", "package_ndc": "72189-222-60", "marketing_start_date": "20210520"}], "brand_name": "ROPINIROLE", "product_id": "72189-222_2c28281e-fe37-b7e4-e063-6294a90ad4f7", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Dopamine Agonists [MoA]", "Nonergot Dopamine Agonist [EPC]"], "product_ndc": "72189-222", "generic_name": "ROPINIROLE", "labeler_name": "DIRECT RX", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ROPINIROLE", "active_ingredients": [{"name": "ROPINIROLE HYDROCHLORIDE", "strength": "1 mg/1"}], "application_number": "ANDA204022", "marketing_category": "ANDA", "marketing_start_date": "20210520", "listing_expiration_date": "20261231"}