Package 72162-2100-1

Brand: clorazepate dipotassium

Generic: clorazepate dipotassium
NDC Package

Package Facts

Identity

Package NDC 72162-2100-1
Digits Only 7216221001
Product NDC 72162-2100
Product ID 72162-2100_3f1acd4a-bbff-4e37-9f42-d05597821589
Description

100 TABLET in 1 BOTTLE (72162-2100-1)

Marketing

Marketing Status
Marketed Since 2022-09-22
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": "3f1acd4a-bbff-4e37-9f42-d05597821589", "openfda": {"unii": ["63FN7G03XY"], "rxcui": ["197464"], "spl_set_id": ["7fccd0b7-1abc-4c52-88e3-af7b7cc079a2"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (72162-2100-1)", "package_ndc": "72162-2100-1", "marketing_start_date": "20220922"}], "brand_name": "Clorazepate Dipotassium", "product_id": "72162-2100_3f1acd4a-bbff-4e37-9f42-d05597821589", "dosage_form": "TABLET", "pharm_class": ["Benzodiazepine [EPC]", "Benzodiazepines [CS]"], "product_ndc": "72162-2100", "dea_schedule": "CIV", "generic_name": "Clorazepate Dipotassium", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Clorazepate Dipotassium", "active_ingredients": [{"name": "CLORAZEPATE DIPOTASSIUM", "strength": "15 mg/1"}], "application_number": "ANDA215566", "marketing_category": "ANDA", "marketing_start_date": "20220922", "listing_expiration_date": "20261231"}