Package 72189-450-60

Brand: alprazolam

Generic: alprazolam
NDC Package

Package Facts

Identity

Package NDC 72189-450-60
Digits Only 7218945060
Product NDC 72189-450
Description

60 TABLET in 1 BOTTLE (72189-450-60)

Marketing

Marketing Status
Marketed Since 2023-03-22
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": "2c4dbbad-3ed5-fec3-e063-6394a90a3b4d", "openfda": {"nui": ["N0000175694", "M0002356"], "unii": ["YU55MQ3IZY"], "rxcui": ["197322"], "spl_set_id": ["f77cfdd0-847d-4edd-e053-6394a90a91b7"], "pharm_class_cs": ["Benzodiazepines [CS]"], "pharm_class_epc": ["Benzodiazepine [EPC]"], "manufacturer_name": ["Direct_Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET in 1 BOTTLE (72189-450-60)", "package_ndc": "72189-450-60", "marketing_start_date": "20230322"}], "brand_name": "Alprazolam", "product_id": "72189-450_2c4dbbad-3ed5-fec3-e063-6394a90a3b4d", "dosage_form": "TABLET", "pharm_class": ["Benzodiazepine [EPC]", "Benzodiazepines [CS]"], "product_ndc": "72189-450", "dea_schedule": "CIV", "generic_name": "Alprazolam", "labeler_name": "Direct_Rx", "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": "20230322", "listing_expiration_date": "20261231"}