Package 72189-637-02

Brand: alprazolam odt c-iv

Generic: alprazolam odt c-iv
NDC Package

Package Facts

Identity

Package NDC 72189-637-02
Digits Only 7218963702
Product NDC 72189-637
Description

2 TABLET, ORALLY DISINTEGRATING in 1 CARTON (72189-637-02)

Marketing

Marketing Status
Marketed Since 2025-08-22
Brand alprazolam odt c-iv
Generic alprazolam odt c-iv
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3cf95203-c8b5-9f06-e063-6394a90abc9c", "openfda": {"nui": ["N0000175694", "M0002356"], "unii": ["YU55MQ3IZY"], "rxcui": ["485415"], "spl_set_id": ["3cf95203-c8b4-9f06-e063-6394a90abc9c"], "pharm_class_cs": ["Benzodiazepines [CS]"], "pharm_class_epc": ["Benzodiazepine [EPC]"], "manufacturer_name": ["Direct_Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "2 TABLET, ORALLY DISINTEGRATING in 1 CARTON (72189-637-02)", "package_ndc": "72189-637-02", "marketing_start_date": "20250822"}], "brand_name": "Alprazolam ODT C-IV", "product_id": "72189-637_3cf95203-c8b5-9f06-e063-6394a90abc9c", "dosage_form": "TABLET, ORALLY DISINTEGRATING", "pharm_class": ["Benzodiazepine [EPC]", "Benzodiazepines [CS]"], "product_ndc": "72189-637", "dea_schedule": "CIV", "generic_name": "Alprazolam ODT C-IV", "labeler_name": "Direct_Rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Alprazolam ODT C-IV", "active_ingredients": [{"name": "ALPRAZOLAM", "strength": ".5 mg/1"}], "application_number": "ANDA078088", "marketing_category": "ANDA", "marketing_start_date": "20250822", "listing_expiration_date": "20261231"}