Package 25021-655-02

Brand: midazolam

Generic: midazolam hydrochloride
NDC Package

Package Facts

Identity

Package NDC 25021-655-02
Digits Only 2502165502
Product NDC 25021-655
Product ID 25021-655_943346c0-d98e-4ac2-a1a2-75427decf2fc
Description

10 VIAL in 1 CARTON (25021-655-02) / 2 mL in 1 VIAL

Marketing

Marketing Status
Marketed Since 2012-03-19
Brand midazolam
Generic midazolam hydrochloride
Sample Package No

Linked Drug Pages (1)

midazolam ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "943346c0-d98e-4ac2-a1a2-75427decf2fc", "openfda": {"unii": ["W7TTW573JJ"], "rxcui": ["1666798"], "spl_set_id": ["e22611dd-1830-40af-9139-7cdb07f5a426"], "manufacturer_name": ["Sagent Pharmaceuticals"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL in 1 CARTON (25021-655-02)  / 2 mL in 1 VIAL", "package_ndc": "25021-655-02", "marketing_start_date": "20120319"}], "brand_name": "midazolam", "product_id": "25021-655_943346c0-d98e-4ac2-a1a2-75427decf2fc", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Benzodiazepine [EPC]", "Benzodiazepines [CS]"], "product_ndc": "25021-655", "dea_schedule": "CIV", "generic_name": "midazolam hydrochloride", "labeler_name": "Sagent Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "midazolam", "active_ingredients": [{"name": "MIDAZOLAM HYDROCHLORIDE", "strength": "1 mg/mL"}], "application_number": "ANDA090696", "marketing_category": "ANDA", "marketing_start_date": "20120319", "listing_expiration_date": "20261231"}