ropinirole

Generic: ropinirole

Labeler: a-s medication solutions
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name ropinirole
Generic Name ropinirole
Labeler a-s medication solutions
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

ropinirole hydrochloride 4 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-7445
Product ID 50090-7445_d8869312-010a-4fa5-a6d4-6df0b21dc881
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA079229
Listing Expiration 2026-12-31
Marketing Start 2022-09-15

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 500907445
Hyphenated Format 50090-7445

Supplemental Identifiers

RxCUI
562704
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 ANDA079229 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 4 mg/1
source: ndc
Packaging
  • 30 TABLET, FILM COATED in 1 BOTTLE (50090-7445-0)
source: ndc

Packages (1)

50090-7445-0 30 TABLET, FILM COATED in 1 BOTTLE (50090-7445-0)

Ingredients (1)

ropinirole hydrochloride (4 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": "d8869312-010a-4fa5-a6d4-6df0b21dc881", "openfda": {"unii": ["D7ZD41RZI9"], "rxcui": ["562704"], "spl_set_id": ["339a961e-4eb0-4406-913e-ccc9e9bde084"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (50090-7445-0)", "package_ndc": "50090-7445-0", "marketing_start_date": "20241106"}], "brand_name": "Ropinirole", "product_id": "50090-7445_d8869312-010a-4fa5-a6d4-6df0b21dc881", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Dopamine Agonists [MoA]", "Nonergot Dopamine Agonist [EPC]"], "product_ndc": "50090-7445", "generic_name": "Ropinirole", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ropinirole", "active_ingredients": [{"name": "ROPINIROLE HYDROCHLORIDE", "strength": "4 mg/1"}], "application_number": "ANDA079229", "marketing_category": "ANDA", "marketing_start_date": "20220915", "listing_expiration_date": "20261231"}