Package 78670-050-96

Brand: lucemyra

Generic: lofexidine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 78670-050-96
Digits Only 7867005096
Product NDC 78670-050
Product ID 78670-050_0be33ddd-71d6-45b7-85ce-e665789911ba
Description

1 BOTTLE in 1 CARTON (78670-050-96) / 96 TABLET, FILM COATED in 1 BOTTLE

Marketing

Marketing Status
Discontinued 2026-08-31
Brand lucemyra
Generic lofexidine hydrochloride
Sample Package No

Linked Drug Pages (1)

Lucemyra ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "0be33ddd-71d6-45b7-85ce-e665789911ba", "openfda": {"unii": ["V47G1SDI1B"], "rxcui": ["2046591", "2046597"], "spl_set_id": ["b748f308-ba71-4fd9-84ec-ec7e0f210885"], "manufacturer_name": ["USWM, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (78670-050-03)  / 36 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "78670-050-03", "marketing_end_date": "20260831", "marketing_start_date": "20210209"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (78670-050-36)  / 36 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "78670-050-36", "marketing_end_date": "20260831", "marketing_start_date": "20210209"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (78670-050-96)  / 96 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "78670-050-96", "marketing_end_date": "20260831", "marketing_start_date": "20210209"}], "brand_name": "Lucemyra", "product_id": "78670-050_0be33ddd-71d6-45b7-85ce-e665789911ba", "dosage_form": "TABLET, FILM COATED", "product_ndc": "78670-050", "generic_name": "lofexidine hydrochloride", "labeler_name": "USWM, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lucemyra", "active_ingredients": [{"name": "LOFEXIDINE HYDROCHLORIDE", "strength": ".2 mg/1"}], "application_number": "NDA209229", "marketing_category": "NDA", "marketing_end_date": "20260831", "marketing_start_date": "20210209"}