Package 72789-256-06

Brand: clorazepate dipotassium

Generic: clorazepate dipotassium
NDC Package

Package Facts

Identity

Package NDC 72789-256-06
Digits Only 7278925606
Product NDC 72789-256
Product ID 72789-256_2e5c9777-8e42-bc90-e063-6294a90a1ee8
Description

6 TABLET in 1 BOTTLE, PLASTIC (72789-256-06)

Marketing

Marketing Status
Marketed Since 2022-07-01
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": "2e5c9777-8e42-bc90-e063-6294a90a1ee8", "openfda": {"unii": ["63FN7G03XY"], "rxcui": ["197464"], "spl_set_id": ["7b59a3ab-3dff-4458-a63a-ef0d9e0d996d"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "6 TABLET in 1 BOTTLE, PLASTIC (72789-256-06)", "package_ndc": "72789-256-06", "marketing_start_date": "20220701"}], "brand_name": "Clorazepate Dipotassium", "product_id": "72789-256_2e5c9777-8e42-bc90-e063-6294a90a1ee8", "dosage_form": "TABLET", "pharm_class": ["Benzodiazepine [EPC]", "Benzodiazepines [CS]"], "product_ndc": "72789-256", "dea_schedule": "CIV", "generic_name": "Clorazepate Dipotassium", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "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": "20000427", "listing_expiration_date": "20261231"}