Package 65862-679-05

Brand: alprazolam

Generic: alprazolam
NDC Package

Package Facts

Identity

Package NDC 65862-679-05
Digits Only 6586267905
Product NDC 65862-679
Description

500 TABLET in 1 BOTTLE (65862-679-05)

Marketing

Marketing Status
Marketed Since 2015-07-31
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": "7527aeb7-8912-404d-afb7-8c692c84422b", "openfda": {"nui": ["N0000175694", "M0002356"], "unii": ["YU55MQ3IZY"], "rxcui": ["197321", "197322", "308047", "308048"], "spl_set_id": ["d2fd0b3e-9b78-44d0-82a6-96d6c6238750"], "pharm_class_cs": ["Benzodiazepines [CS]"], "pharm_class_epc": ["Benzodiazepine [EPC]"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (65862-679-01)", "package_ndc": "65862-679-01", "marketing_start_date": "20150731"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (65862-679-05)", "package_ndc": "65862-679-05", "marketing_start_date": "20150731"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (65862-679-99)", "package_ndc": "65862-679-99", "marketing_start_date": "20150731"}], "brand_name": "Alprazolam", "product_id": "65862-679_7527aeb7-8912-404d-afb7-8c692c84422b", "dosage_form": "TABLET", "pharm_class": ["Benzodiazepine [EPC]", "Benzodiazepines [CS]"], "product_ndc": "65862-679", "dea_schedule": "CIV", "generic_name": "Alprazolam", "labeler_name": "Aurobindo Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Alprazolam", "active_ingredients": [{"name": "ALPRAZOLAM", "strength": "2 mg/1"}], "application_number": "ANDA203346", "marketing_category": "ANDA", "marketing_start_date": "20150731", "listing_expiration_date": "20261231"}