Package 76420-665-90

Brand: alprazolam

Generic: alprazolam
NDC Package

Package Facts

Identity

Package NDC 76420-665-90
Digits Only 7642066590
Product NDC 76420-665
Description

90 TABLET in 1 BOTTLE (76420-665-90)

Marketing

Marketing Status
Marketed Since 2024-01-11
Brand alprazolam
Generic alprazolam
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "0ea9692e-7d75-80f3-e063-6294a90ad6f9", "openfda": {"nui": ["N0000175694", "M0002356"], "unii": ["YU55MQ3IZY"], "rxcui": ["197321", "197322", "308047", "308048"], "spl_set_id": ["e3245259-024f-4bd9-9ec6-94aa11febfd7"], "pharm_class_cs": ["Benzodiazepines [CS]"], "pharm_class_epc": ["Benzodiazepine [EPC]"], "manufacturer_name": ["Asclemed USA, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (76420-665-01)", "package_ndc": "76420-665-01", "marketing_start_date": "20240111"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (76420-665-30)", "package_ndc": "76420-665-30", "marketing_start_date": "20240111"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (76420-665-60)", "package_ndc": "76420-665-60", "marketing_start_date": "20240111"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (76420-665-90)", "package_ndc": "76420-665-90", "marketing_start_date": "20240111"}], "brand_name": "Alprazolam", "product_id": "76420-665_0ea9692e-7d75-80f3-e063-6294a90ad6f9", "dosage_form": "TABLET", "pharm_class": ["Benzodiazepine [EPC]", "Benzodiazepines [CS]"], "product_ndc": "76420-665", "dea_schedule": "CIV", "generic_name": "alprazolam", "labeler_name": "Asclemed USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Alprazolam", "active_ingredients": [{"name": "ALPRAZOLAM", "strength": ".5 mg/1"}], "application_number": "NDA018276", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "19811016", "listing_expiration_date": "20261231"}