Package 72603-114-01

Brand: clorazepate dipotassium

Generic: clorazepate dipotassium
NDC Package

Package Facts

Identity

Package NDC 72603-114-01
Digits Only 7260311401
Product NDC 72603-114
Product ID 72603-114_258be954-8e31-2be4-e063-6394a90a78ca
Description

100 TABLET in 1 BOTTLE (72603-114-01)

Marketing

Marketing Status
Marketed Since 2022-10-24
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": "258be954-8e31-2be4-e063-6394a90a78ca", "openfda": {"unii": ["63FN7G03XY"], "rxcui": ["197464", "197465", "197466"], "spl_set_id": ["fb5c9e98-02b2-4c36-b436-25b58fe3c7d5"], "manufacturer_name": ["NORTHSTAR RX LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (72603-114-01)", "package_ndc": "72603-114-01", "marketing_start_date": "20221024"}], "brand_name": "Clorazepate Dipotassium", "product_id": "72603-114_258be954-8e31-2be4-e063-6394a90a78ca", "dosage_form": "TABLET", "pharm_class": ["Benzodiazepine [EPC]", "Benzodiazepines [CS]"], "product_ndc": "72603-114", "dea_schedule": "CIV", "generic_name": "Clorazepate Dipotassium", "labeler_name": "NORTHSTAR RX LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Clorazepate Dipotassium", "active_ingredients": [{"name": "CLORAZEPATE DIPOTASSIUM", "strength": "15 mg/1"}], "application_number": "ANDA075731", "marketing_category": "ANDA", "marketing_start_date": "20221024", "listing_expiration_date": "20261231"}