Package 71921-250-96

Brand: lofexidine

Generic: lofexidine
NDC Package

Package Facts

Identity

Package NDC 71921-250-96
Digits Only 7192125096
Product NDC 71921-250
Product ID 71921-250_ce4488e2-842c-45ba-aca7-075a900e2a1c
Description

1 BOTTLE in 1 CARTON (71921-250-96) / 96 TABLET, COATED in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2024-08-21
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": "ce4488e2-842c-45ba-aca7-075a900e2a1c", "openfda": {"unii": ["V47G1SDI1B"], "rxcui": ["2046591"], "spl_set_id": ["ce4488e2-842c-45ba-aca7-075a900e2a1c"], "manufacturer_name": ["Florida Pharmaceutical Products, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (71921-250-36)  / 36 TABLET, COATED in 1 BOTTLE", "package_ndc": "71921-250-36", "marketing_start_date": "20240821"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (71921-250-96)  / 96 TABLET, COATED in 1 BOTTLE", "package_ndc": "71921-250-96", "marketing_start_date": "20240821"}], "brand_name": "Lofexidine", "product_id": "71921-250_ce4488e2-842c-45ba-aca7-075a900e2a1c", "dosage_form": "TABLET, COATED", "product_ndc": "71921-250", "generic_name": "Lofexidine", "labeler_name": "Florida Pharmaceutical Products, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lofexidine", "active_ingredients": [{"name": "LOFEXIDINE HYDROCHLORIDE", "strength": ".18 mg/1"}], "application_number": "ANDA218613", "marketing_category": "ANDA", "marketing_start_date": "20240821", "listing_expiration_date": "20261231"}