Package 80425-0120-2

Brand: diazepam

Generic: diazepam
NDC Package

Package Facts

Identity

Package NDC 80425-0120-2
Digits Only 8042501202
Product NDC 80425-0120
Product ID 80425-0120_2a999573-1032-813a-e063-6294a90a49b1
Description

60 TABLET in 1 BOTTLE (80425-0120-2)

Marketing

Marketing Status
Marketed Since 1986-12-10
Brand diazepam
Generic diazepam
Sample Package No

Linked Drug Pages (1)

Diazepam ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "2a999573-1032-813a-e063-6294a90a49b1", "openfda": {"nui": ["N0000175694", "M0002356"], "unii": ["Q3JTX2Q7TU"], "rxcui": ["197589"], "spl_set_id": ["b7002d26-3856-4c2f-e053-2995a90aea60"], "pharm_class_cs": ["Benzodiazepines [CS]"], "pharm_class_epc": ["Benzodiazepine [EPC]"], "manufacturer_name": ["Advanced Rx Pharmacy of Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET in 1 BOTTLE (80425-0120-2)", "package_ndc": "80425-0120-2", "marketing_start_date": "19861210"}], "brand_name": "Diazepam", "product_id": "80425-0120_2a999573-1032-813a-e063-6294a90a49b1", "dosage_form": "TABLET", "pharm_class": ["Benzodiazepine [EPC]", "Benzodiazepines [CS]"], "product_ndc": "80425-0120", "dea_schedule": "CIV", "generic_name": "Diazepam", "labeler_name": "Advanced Rx Pharmacy of Tennessee, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Diazepam", "active_ingredients": [{"name": "DIAZEPAM", "strength": "10 mg/1"}], "application_number": "ANDA071322", "marketing_category": "ANDA", "marketing_start_date": "19861210", "listing_expiration_date": "20261231"}