Package 66993-345-76

Brand: lofexidine hydrochloride

Generic: lofexidine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 66993-345-76
Digits Only 6699334576
Product NDC 66993-345
Product ID 66993-345_b317fb7f-8a02-4d11-9d20-401644e5d6ef
Description

1 BOTTLE in 1 CARTON (66993-345-76) / 96 TABLET, FILM COATED in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2024-08-29
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": "b317fb7f-8a02-4d11-9d20-401644e5d6ef", "openfda": {"unii": ["V47G1SDI1B"], "rxcui": ["2046591"], "spl_set_id": ["77367dfa-434f-4d61-95fe-f0f1628457d1"], "manufacturer_name": ["Prasco Laboratories"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (66993-345-37)  / 36 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "66993-345-37", "marketing_start_date": "20240829"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (66993-345-76)  / 96 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "66993-345-76", "marketing_start_date": "20240829"}], "brand_name": "Lofexidine hydrochloride", "product_id": "66993-345_b317fb7f-8a02-4d11-9d20-401644e5d6ef", "dosage_form": "TABLET, FILM COATED", "product_ndc": "66993-345", "generic_name": "lofexidine hydrochloride", "labeler_name": "Prasco Laboratories", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lofexidine hydrochloride", "active_ingredients": [{"name": "LOFEXIDINE HYDROCHLORIDE", "strength": ".2 mg/1"}], "application_number": "NDA209229", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20240829", "listing_expiration_date": "20261231"}