Package 0259-5010-60

Brand: ampyra

Generic: dalfampridine
NDC Package

Package Facts

Identity

Package NDC 0259-5010-60
Digits Only 0259501060
Product NDC 0259-5010
Description

60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0259-5010-60)

Marketing

Marketing Status
Marketed Since 2010-03-01
Brand ampyra
Generic dalfampridine
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "b0f65c2b-ee14-421f-9f24-178e108e38cf", "openfda": {"nui": ["N0000192795", "N0000175448"], "unii": ["BH3B64OKL9"], "rxcui": ["897021", "897025"], "spl_set_id": ["974fb2af-7012-4989-b330-e44a31c9c3e5"], "pharm_class_epc": ["Potassium Channel Blocker [EPC]"], "pharm_class_moa": ["Potassium Channel Antagonists [MoA]"], "manufacturer_name": ["Merz Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0259-5010-60)", "package_ndc": "0259-5010-60", "marketing_start_date": "20100301"}], "brand_name": "AMPYRA", "product_id": "0259-5010_b0f65c2b-ee14-421f-9f24-178e108e38cf", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Potassium Channel Antagonists [MoA]", "Potassium Channel Blocker [EPC]"], "product_ndc": "0259-5010", "generic_name": "Dalfampridine", "labeler_name": "Merz Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "AMPYRA", "active_ingredients": [{"name": "DALFAMPRIDINE", "strength": "10 mg/1"}], "application_number": "NDA022250", "marketing_category": "NDA", "marketing_start_date": "20100301", "listing_expiration_date": "20261231"}