Package 76420-316-90

Brand: diazepam

Generic: diazepam
NDC Package

Package Facts

Identity

Package NDC 76420-316-90
Digits Only 7642031690
Product NDC 76420-316
Description

90 TABLET in 1 BOTTLE (76420-316-90)

Marketing

Marketing Status
Marketed Since 2025-10-31
Brand diazepam
Generic diazepam
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "42708657-5977-a009-e063-6294a90a3919", "openfda": {"nui": ["N0000175694", "M0002356"], "unii": ["Q3JTX2Q7TU"], "rxcui": ["197589", "197590", "197591"], "spl_set_id": ["426f3da1-4105-ba0a-e063-6294a90a7a86"], "pharm_class_cs": ["Benzodiazepines [CS]"], "pharm_class_epc": ["Benzodiazepine [EPC]"], "manufacturer_name": ["ASCLEMED USA INC."]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET in 1 BOTTLE (76420-316-00)", "package_ndc": "76420-316-00", "marketing_start_date": "20251031"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (76420-316-01)", "package_ndc": "76420-316-01", "marketing_start_date": "20251031"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (76420-316-05)", "package_ndc": "76420-316-05", "marketing_start_date": "20251031"}, {"sample": false, "description": "10 TABLET in 1 BOTTLE (76420-316-10)", "package_ndc": "76420-316-10", "marketing_start_date": "20251031"}, {"sample": false, "description": "20 TABLET in 1 BOTTLE (76420-316-20)", "package_ndc": "76420-316-20", "marketing_start_date": "20251031"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (76420-316-30)", "package_ndc": "76420-316-30", "marketing_start_date": "20251031"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (76420-316-60)", "package_ndc": "76420-316-60", "marketing_start_date": "20251031"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (76420-316-90)", "package_ndc": "76420-316-90", "marketing_start_date": "20251031"}], "brand_name": "DIAZEPAM", "product_id": "76420-316_42708657-5977-a009-e063-6294a90a3919", "dosage_form": "TABLET", "pharm_class": ["Benzodiazepine [EPC]", "Benzodiazepines [CS]"], "product_ndc": "76420-316", "dea_schedule": "CIV", "generic_name": "DIAZEPAM", "labeler_name": "ASCLEMED USA INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "DIAZEPAM", "active_ingredients": [{"name": "DIAZEPAM", "strength": "10 mg/1"}], "application_number": "ANDA217843", "marketing_category": "ANDA", "marketing_start_date": "20231214", "listing_expiration_date": "20261231"}