Package 0172-3926-70

Brand: diazepam

Generic: diazepam
NDC Package

Package Facts

Identity

Package NDC 0172-3926-70
Digits Only 0172392670
Product NDC 0172-3926
Product ID 0172-3926_db225e5f-9265-4460-ab58-3305246c6258
Description

500 TABLET in 1 BOTTLE (0172-3926-70)

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": "db225e5f-9265-4460-ab58-3305246c6258", "openfda": {"nui": ["N0000175694", "M0002356"], "upc": ["0301723926609", "0301723927606", "0301723925602"], "unii": ["Q3JTX2Q7TU"], "rxcui": ["197589", "197590", "197591"], "spl_set_id": ["48aa32cb-047a-414a-822e-82a5f26d8817"], "pharm_class_cs": ["Benzodiazepines [CS]"], "pharm_class_epc": ["Benzodiazepine [EPC]"], "manufacturer_name": ["Teva Pharmaceuticals USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (0172-3926-60)", "package_ndc": "0172-3926-60", "marketing_start_date": "19861210"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (0172-3926-70)", "package_ndc": "0172-3926-70", "marketing_start_date": "19861210"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (0172-3926-80)", "package_ndc": "0172-3926-80", "marketing_start_date": "19861210"}], "brand_name": "Diazepam", "product_id": "0172-3926_db225e5f-9265-4460-ab58-3305246c6258", "dosage_form": "TABLET", "pharm_class": ["Benzodiazepine [EPC]", "Benzodiazepines [CS]"], "product_ndc": "0172-3926", "dea_schedule": "CIV", "generic_name": "Diazepam", "labeler_name": "Teva Pharmaceuticals USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Diazepam", "active_ingredients": [{"name": "DIAZEPAM", "strength": "5 mg/1"}], "application_number": "ANDA071321", "marketing_category": "ANDA", "marketing_start_date": "19861210", "listing_expiration_date": "20261231"}