Package 68071-3817-1

Brand: alprazolam

Generic: alprazolam
NDC Package

Package Facts

Identity

Package NDC 68071-3817-1
Digits Only 6807138171
Product NDC 68071-3817
Description

1000 TABLET in 1 BOTTLE (68071-3817-1)

Marketing

Marketing Status
Marketed Since 2025-03-27
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": "315b67a4-d076-3c01-e063-6394a90a172d", "openfda": {"nui": ["N0000175694", "M0002356"], "upc": ["0368071381719"], "unii": ["YU55MQ3IZY"], "rxcui": ["308047"], "spl_set_id": ["315b5782-969a-4324-e063-6394a90acf37"], "pharm_class_cs": ["Benzodiazepines [CS]"], "pharm_class_epc": ["Benzodiazepine [EPC]"], "manufacturer_name": ["NuCare Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET in 1 BOTTLE (68071-3817-1)", "package_ndc": "68071-3817-1", "marketing_start_date": "20250327"}], "brand_name": "Alprazolam", "product_id": "68071-3817_315b67a4-d076-3c01-e063-6394a90a172d", "dosage_form": "TABLET", "pharm_class": ["Benzodiazepine [EPC]", "Benzodiazepines [CS]"], "product_ndc": "68071-3817", "dea_schedule": "CIV", "generic_name": "Alprazolam", "labeler_name": "NuCare Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Alprazolam", "active_ingredients": [{"name": "ALPRAZOLAM", "strength": ".25 mg/1"}], "application_number": "ANDA203346", "marketing_category": "ANDA", "marketing_start_date": "20150731", "listing_expiration_date": "20261231"}