Package 82249-702-60

Brand: dalfampridine

Generic: dalfampridine
NDC Package

Package Facts

Identity

Package NDC 82249-702-60
Digits Only 8224970260
Product NDC 82249-702
Description

60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (82249-702-60)

Marketing

Marketing Status
Marketed Since 2025-07-21
Brand dalfampridine
Generic dalfampridine
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "c40dcc84-b839-44aa-94f2-886fb1c3d75c", "openfda": {"nui": ["N0000192795", "N0000175448"], "unii": ["BH3B64OKL9"], "rxcui": ["897021"], "spl_set_id": ["c40dcc84-b839-44aa-94f2-886fb1c3d75c"], "pharm_class_epc": ["Potassium Channel Blocker [EPC]"], "pharm_class_moa": ["Potassium Channel Antagonists [MoA]"], "manufacturer_name": ["CivicaScript LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (82249-702-60)", "package_ndc": "82249-702-60", "marketing_start_date": "20250721"}], "brand_name": "Dalfampridine", "product_id": "82249-702_c40dcc84-b839-44aa-94f2-886fb1c3d75c", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Potassium Channel Antagonists [MoA]", "Potassium Channel Blocker [EPC]"], "product_ndc": "82249-702", "generic_name": "Dalfampridine", "labeler_name": "CivicaScript LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Dalfampridine", "active_ingredients": [{"name": "DALFAMPRIDINE", "strength": "10 mg/1"}], "application_number": "ANDA206765", "marketing_category": "ANDA", "marketing_start_date": "20250721", "listing_expiration_date": "20261231"}