Package 70518-4137-0

Brand: alprazolam

Generic: alprazolam
NDC Package

Package Facts

Identity

Package NDC 70518-4137-0
Digits Only 7051841370
Product NDC 70518-4137
Product ID 70518-4137_1cf8baf2-ee1d-a98b-e063-6394a90a0c81
Description

60 TABLET in 1 BOTTLE, PLASTIC (70518-4137-0)

Marketing

Marketing Status
Discontinued 2027-03-19
Brand alprazolam
Generic alprazolam
Sample Package No

Linked Drug Pages (1)

Alprazolam ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "1cf8baf2-ee1d-a98b-e063-6394a90a0c81", "openfda": {"nui": ["N0000175694", "M0002356"], "unii": ["YU55MQ3IZY"], "rxcui": ["197321"], "spl_set_id": ["563e09db-2f3d-4ce8-b356-ae44477be6d0"], "pharm_class_cs": ["Benzodiazepines [CS]"], "pharm_class_epc": ["Benzodiazepine [EPC]"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET in 1 BOTTLE, PLASTIC (70518-4137-0)", "package_ndc": "70518-4137-0", "marketing_end_date": "20270319", "marketing_start_date": "20240710"}], "brand_name": "Alprazolam", "product_id": "70518-4137_1cf8baf2-ee1d-a98b-e063-6394a90a0c81", "dosage_form": "TABLET", "pharm_class": ["Benzodiazepine [EPC]", "Benzodiazepines [CS]"], "product_ndc": "70518-4137", "dea_schedule": "CIV", "generic_name": "Alprazolam", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Alprazolam", "active_ingredients": [{"name": "ALPRAZOLAM", "strength": "1 mg/1"}], "application_number": "ANDA074112", "marketing_category": "ANDA", "marketing_end_date": "20270319", "marketing_start_date": "20240710"}