Package 70954-909-10

Brand: lofexidine

Generic: lofexidine
NDC Package

Package Facts

Identity

Package NDC 70954-909-10
Digits Only 7095490910
Product NDC 70954-909
Product ID 70954-909_335e26bf-b236-46d6-81cf-2879e5f3b1d9
Description

36 TABLET in 1 BOTTLE (70954-909-10)

Marketing

Marketing Status
Marketed Since 2025-10-22
Brand lofexidine
Generic lofexidine
Sample Package No

Linked Drug Pages (1)

Lofexidine ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "335e26bf-b236-46d6-81cf-2879e5f3b1d9", "openfda": {"upc": ["0370954909200", "0370954909101"], "unii": ["V47G1SDI1B"], "rxcui": ["2046591"], "spl_set_id": ["335e26bf-b236-46d6-81cf-2879e5f3b1d9"], "manufacturer_name": ["ANI Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "36 TABLET in 1 BOTTLE (70954-909-10)", "package_ndc": "70954-909-10", "marketing_start_date": "20251022"}, {"sample": false, "description": "96 TABLET in 1 BOTTLE (70954-909-20)", "package_ndc": "70954-909-20", "marketing_start_date": "20251022"}], "brand_name": "Lofexidine", "product_id": "70954-909_335e26bf-b236-46d6-81cf-2879e5f3b1d9", "dosage_form": "TABLET", "product_ndc": "70954-909", "generic_name": "Lofexidine", "labeler_name": "ANI Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lofexidine", "active_ingredients": [{"name": "LOFEXIDINE HYDROCHLORIDE", "strength": ".18 mg/1"}], "application_number": "ANDA219917", "marketing_category": "ANDA", "marketing_start_date": "20251022", "listing_expiration_date": "20261231"}