Package 62332-035-31

Brand: ropinirole

Generic: ropinirole
NDC Package

Package Facts

Identity

Package NDC 62332-035-31
Digits Only 6233203531
Product NDC 62332-035
Description

100 TABLET, FILM COATED in 1 BOTTLE (62332-035-31)

Marketing

Marketing Status
Marketed Since 2016-01-29
Brand ropinirole
Generic ropinirole
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "061e4779-5a53-4782-bb85-03abe1c98ce1", "openfda": {"upc": ["0362332031313", "0362332032310", "0362332035311", "0362332033317", "0362332034314", "0362332036318", "0362332030316"], "unii": ["D7ZD41RZI9"], "rxcui": ["283858", "312845", "312846", "312847", "312849", "314208", "562704"], "spl_set_id": ["6d1a0f9f-5fa0-43fa-83b9-0d18a129fd0c"], "manufacturer_name": ["Alembic Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (62332-035-31)", "package_ndc": "62332-035-31", "marketing_start_date": "20160129"}], "brand_name": "ROPINIROLE", "product_id": "62332-035_061e4779-5a53-4782-bb85-03abe1c98ce1", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Dopamine Agonists [MoA]", "Nonergot Dopamine Agonist [EPC]"], "product_ndc": "62332-035", "generic_name": "ROPINIROLE", "labeler_name": "Alembic Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ROPINIROLE", "active_ingredients": [{"name": "ROPINIROLE HYDROCHLORIDE", "strength": "4 mg/1"}], "application_number": "ANDA090429", "marketing_category": "ANDA", "marketing_start_date": "20160129", "listing_expiration_date": "20261231"}