Package 0140-0004-01

Brand: valium

Generic: diazepam
NDC Package

Package Facts

Identity

Package NDC 0140-0004-01
Digits Only 0140000401
Product NDC 0140-0004
Description

1 BOTTLE, PLASTIC in 1 CARTON (0140-0004-01) / 100 TABLET in 1 BOTTLE, PLASTIC

Marketing

Marketing Status
Discontinued 2027-08-10
Brand valium
Generic diazepam
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "ea505cdb-6d89-4b8c-8007-ec5a5fe920ce", "openfda": {"nui": ["N0000175694", "M0002356"], "unii": ["Q3JTX2Q7TU"], "rxcui": ["104699", "104700", "197590", "197591"], "spl_set_id": ["554baee5-b171-4452-a50a-41a0946f956c"], "pharm_class_cs": ["Benzodiazepines [CS]"], "pharm_class_epc": ["Benzodiazepine [EPC]"], "manufacturer_name": ["Roche Laboratories Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (0140-0004-01)  / 100 TABLET in 1 BOTTLE, PLASTIC", "package_ndc": "0140-0004-01", "marketing_end_date": "20270810", "marketing_start_date": "19631115"}], "brand_name": "Valium", "product_id": "0140-0004_ea505cdb-6d89-4b8c-8007-ec5a5fe920ce", "dosage_form": "TABLET", "pharm_class": ["Benzodiazepine [EPC]", "Benzodiazepines [CS]"], "product_ndc": "0140-0004", "dea_schedule": "CIV", "generic_name": "diazepam", "labeler_name": "Roche Laboratories Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Valium", "active_ingredients": [{"name": "DIAZEPAM", "strength": "2 mg/1"}], "application_number": "NDA013263", "marketing_category": "NDA", "marketing_end_date": "20270810", "marketing_start_date": "19631115"}