Package 10135-679-01

Brand: ropinirole

Generic: ropinirole
NDC Package

Package Facts

Identity

Package NDC 10135-679-01
Digits Only 1013567901
Product NDC 10135-679
Product ID 10135-679_441e0572-3413-1a21-e063-6294a90a8e6a
Description

100 TABLET, FILM COATED in 1 BOTTLE (10135-679-01)

Marketing

Marketing Status
Marketed Since 2019-03-15
Brand ropinirole
Generic ropinirole
Sample Package No

Linked Drug Pages (1)

Ropinirole ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "441e0572-3413-1a21-e063-6294a90a8e6a", "openfda": {"unii": ["D7ZD41RZI9"], "rxcui": ["283858", "312845", "312846", "312847", "312849", "314208", "562704"], "spl_set_id": ["35d90f6f-3116-4afa-be2d-b65c160e8ab3"], "manufacturer_name": ["Marlex Pharmaceuticals Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (10135-679-01)", "package_ndc": "10135-679-01", "marketing_start_date": "20190315"}], "brand_name": "Ropinirole", "product_id": "10135-679_441e0572-3413-1a21-e063-6294a90a8e6a", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Dopamine Agonists [MoA]", "Nonergot Dopamine Agonist [EPC]"], "product_ndc": "10135-679", "generic_name": "ropinirole", "labeler_name": "Marlex Pharmaceuticals Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ropinirole", "active_ingredients": [{"name": "ROPINIROLE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA079165", "marketing_category": "ANDA", "marketing_start_date": "20190315", "listing_expiration_date": "20261231"}