Package 67046-1462-3

Brand: clorazepate dipotassium

Generic: clorazepate dipotassium
NDC Package

Package Facts

Identity

Package NDC 67046-1462-3
Digits Only 6704614623
Product NDC 67046-1462
Product ID 67046-1462_2d5938fe-3981-3cd5-e063-6394a90a99a9
Description

30 TABLET in 1 BLISTER PACK (67046-1462-3)

Marketing

Marketing Status
Marketed Since 2025-02-04
Brand clorazepate dipotassium
Generic clorazepate dipotassium
Sample Package No

Linked Drug Pages (1)

Clorazepate Dipotassium ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "2d5938fe-3981-3cd5-e063-6394a90a99a9", "openfda": {"unii": ["63FN7G03XY"], "rxcui": ["197464"], "spl_set_id": ["2d592a27-f4cf-008a-e063-6394a90a2629"], "manufacturer_name": ["Coupler LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (67046-1462-3)", "package_ndc": "67046-1462-3", "marketing_start_date": "20250204"}], "brand_name": "Clorazepate Dipotassium", "product_id": "67046-1462_2d5938fe-3981-3cd5-e063-6394a90a99a9", "dosage_form": "TABLET", "pharm_class": ["Benzodiazepine [EPC]", "Benzodiazepines [CS]"], "product_ndc": "67046-1462", "dea_schedule": "CIV", "generic_name": "Clorazepate Dipotassium", "labeler_name": "Coupler LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Clorazepate Dipotassium", "active_ingredients": [{"name": "CLORAZEPATE DIPOTASSIUM", "strength": "15 mg/1"}], "application_number": "ANDA213730", "marketing_category": "ANDA", "marketing_start_date": "20250204", "listing_expiration_date": "20261231"}