Package 72189-570-30

Brand: diazepam

Generic: diazepam
NDC Package

Package Facts

Identity

Package NDC 72189-570-30
Digits Only 7218957030
Product NDC 72189-570
Product ID 72189-570_2047f721-6a06-c391-e063-6394a90a4ed7
Description

30 TABLET in 1 BOTTLE, PLASTIC (72189-570-30)

Marketing

Marketing Status
Marketed Since 2024-08-22
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": "2047f721-6a06-c391-e063-6394a90a4ed7", "openfda": {"nui": ["N0000175694", "M0002356"], "unii": ["Q3JTX2Q7TU"], "rxcui": ["197590"], "spl_set_id": ["2047f721-6a05-c391-e063-6394a90a4ed7"], "pharm_class_cs": ["Benzodiazepines [CS]"], "pharm_class_epc": ["Benzodiazepine [EPC]"], "manufacturer_name": ["Direct_rx"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (72189-570-30)", "package_ndc": "72189-570-30", "marketing_start_date": "20240822"}], "brand_name": "Diazepam", "product_id": "72189-570_2047f721-6a06-c391-e063-6394a90a4ed7", "dosage_form": "TABLET", "pharm_class": ["Benzodiazepine [EPC]", "Benzodiazepines [CS]"], "product_ndc": "72189-570", "dea_schedule": "CIV", "generic_name": "Diazepam", "labeler_name": "Direct_rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Diazepam", "active_ingredients": [{"name": "DIAZEPAM", "strength": "2 mg/1"}], "application_number": "ANDA070325", "marketing_category": "ANDA", "marketing_start_date": "20240822", "listing_expiration_date": "20261231"}