Package 72205-246-43

Brand: lofexidine hydrochloride

Generic: lofexidine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72205-246-43
Digits Only 7220524643
Product NDC 72205-246
Product ID 72205-246_19b5c932-af2d-4a0b-ac4a-ba06c53c3219
Description

1 BOTTLE in 1 CARTON (72205-246-43) / 96 TABLET, FILM COATED in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2025-03-01
Brand lofexidine hydrochloride
Generic lofexidine hydrochloride
Sample Package No

Linked Drug Pages (1)

lofexidine hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "19b5c932-af2d-4a0b-ac4a-ba06c53c3219", "openfda": {"upc": ["0372205246430", "0372205246423"], "unii": ["V47G1SDI1B"], "rxcui": ["2046591"], "spl_set_id": ["19b5c932-af2d-4a0b-ac4a-ba06c53c3219"], "manufacturer_name": ["Novadoz Pharmaceuticals LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (72205-246-42)  / 36 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "72205-246-42", "marketing_start_date": "20250301"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (72205-246-43)  / 96 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "72205-246-43", "marketing_start_date": "20250301"}], "brand_name": "lofexidine hydrochloride", "product_id": "72205-246_19b5c932-af2d-4a0b-ac4a-ba06c53c3219", "dosage_form": "TABLET, FILM COATED", "product_ndc": "72205-246", "generic_name": "lofexidine hydrochloride", "labeler_name": "Novadoz Pharmaceuticals LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "lofexidine hydrochloride", "active_ingredients": [{"name": "LOFEXIDINE HYDROCHLORIDE", "strength": ".2 mg/1"}], "application_number": "ANDA218699", "marketing_category": "ANDA", "marketing_start_date": "20250224", "listing_expiration_date": "20261231"}