Package 11534-202-03

Brand: diazepam

Generic: diazepam
NDC Package

Package Facts

Identity

Package NDC 11534-202-03
Digits Only 1153420203
Product NDC 11534-202
Description

1000 TABLET in 1 BOTTLE (11534-202-03)

Marketing

Marketing Status
Marketed Since 2024-12-10
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": "e95b8ea6-9d51-4621-bb87-a365121b08bb", "openfda": {"nui": ["N0000175694", "M0002356"], "unii": ["Q3JTX2Q7TU"], "rxcui": ["197589", "197590", "197591"], "spl_set_id": ["34ac0b9d-d4ad-4aaa-8bee-902365f4e9a8"], "pharm_class_cs": ["Benzodiazepines [CS]"], "pharm_class_epc": ["Benzodiazepine [EPC]"], "manufacturer_name": ["Sunrise Pharmaceutical, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (11534-202-01)", "package_ndc": "11534-202-01", "marketing_start_date": "20241210"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (11534-202-03)", "package_ndc": "11534-202-03", "marketing_start_date": "20241210"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (11534-202-04)", "package_ndc": "11534-202-04", "marketing_start_date": "20241210"}], "brand_name": "DIAZEPAM", "product_id": "11534-202_e95b8ea6-9d51-4621-bb87-a365121b08bb", "dosage_form": "TABLET", "pharm_class": ["Benzodiazepine [EPC]", "Benzodiazepines [CS]"], "product_ndc": "11534-202", "dea_schedule": "CIV", "generic_name": "diazepam", "labeler_name": "Sunrise Pharmaceutical, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "DIAZEPAM", "active_ingredients": [{"name": "DIAZEPAM", "strength": "2 mg/1"}], "application_number": "ANDA070464", "marketing_category": "ANDA", "marketing_start_date": "20241209", "listing_expiration_date": "20261231"}