Package 13107-320-05

Brand: clorazepate dipotassium

Generic: clorazepate dipotassium
NDC Package

Package Facts

Identity

Package NDC 13107-320-05
Digits Only 1310732005
Product NDC 13107-320
Product ID 13107-320_c9a14da8-3888-4f13-b695-0005240d8300
Description

500 TABLET in 1 BOTTLE, PLASTIC (13107-320-05)

Marketing

Marketing Status
Marketed Since 1987-07-17
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": "c9a14da8-3888-4f13-b695-0005240d8300", "openfda": {"upc": ["0313107321016", "0313107320019", "0313107319013"], "unii": ["63FN7G03XY"], "rxcui": ["197464", "197465", "197466"], "spl_set_id": ["919cbd07-f587-4005-acff-26213dd1d1fb"], "manufacturer_name": ["Aurolife Pharma, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (13107-320-01)", "package_ndc": "13107-320-01", "marketing_start_date": "19870717"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE, PLASTIC (13107-320-05)", "package_ndc": "13107-320-05", "marketing_start_date": "19870717"}], "brand_name": "CLORAZEPATE DIPOTASSIUM", "product_id": "13107-320_c9a14da8-3888-4f13-b695-0005240d8300", "dosage_form": "TABLET", "pharm_class": ["Benzodiazepine [EPC]", "Benzodiazepines [CS]"], "product_ndc": "13107-320", "dea_schedule": "CIV", "generic_name": "CLORAZEPATE DIPOTASSIUM", "labeler_name": "Aurolife Pharma, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "CLORAZEPATE DIPOTASSIUM", "active_ingredients": [{"name": "CLORAZEPATE DIPOTASSIUM", "strength": "7.5 mg/1"}], "application_number": "ANDA071858", "marketing_category": "ANDA", "marketing_start_date": "19870717", "listing_expiration_date": "20261231"}