Package 67046-1601-3

Brand: clorazepate dipotassium

Generic: clorazepate dipotassium
NDC Package

Package Facts

Identity

Package NDC 67046-1601-3
Digits Only 6704616013
Product NDC 67046-1601
Product ID 67046-1601_40074e64-23a7-50b1-e063-6294a90a92c6
Description

30 TABLET in 1 BLISTER PACK (67046-1601-3)

Marketing

Marketing Status
Marketed Since 2025-09-30
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": "40074e64-23a7-50b1-e063-6294a90a92c6", "openfda": {"unii": ["63FN7G03XY"], "rxcui": ["197466"], "spl_set_id": ["40074ed8-0799-e3e0-e063-6394a90ad200"], "manufacturer_name": ["Coupler LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (67046-1601-3)", "package_ndc": "67046-1601-3", "marketing_start_date": "20250930"}], "brand_name": "Clorazepate Dipotassium", "product_id": "67046-1601_40074e64-23a7-50b1-e063-6294a90a92c6", "dosage_form": "TABLET", "pharm_class": ["Benzodiazepine [EPC]", "Benzodiazepines [CS]"], "product_ndc": "67046-1601", "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": "7.5 mg/1"}], "application_number": "ANDA075731", "marketing_category": "ANDA", "marketing_start_date": "20250930", "listing_expiration_date": "20261231"}