Package 0404-9913-05

Brand: midazolam

Generic: midazolam
NDC Package

Package Facts

Identity

Package NDC 0404-9913-05
Digits Only 0404991305
Product NDC 0404-9913
Description

1 VIAL in 1 BAG (0404-9913-05) / 5 mL in 1 VIAL

Marketing

Marketing Status
Marketed Since 2022-01-13
Brand midazolam
Generic midazolam
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "09538099-2828-4215-9a17-3b9a100134cd", "openfda": {"unii": ["W7TTW573JJ"], "rxcui": ["311700"], "spl_set_id": ["3c2fd6ee-4ede-4ee4-8c05-34c93598f381"], "manufacturer_name": ["Henry Schein, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 BAG (0404-9913-05)  / 5 mL in 1 VIAL", "package_ndc": "0404-9913-05", "marketing_start_date": "20220113"}], "brand_name": "Midazolam", "product_id": "0404-9913_09538099-2828-4215-9a17-3b9a100134cd", "dosage_form": "INJECTION", "pharm_class": ["Benzodiazepine [EPC]", "Benzodiazepines [CS]"], "product_ndc": "0404-9913", "dea_schedule": "CIV", "generic_name": "Midazolam", "labeler_name": "Henry Schein, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Midazolam", "active_ingredients": [{"name": "MIDAZOLAM HYDROCHLORIDE", "strength": "1 mg/mL"}], "application_number": "ANDA075243", "marketing_category": "ANDA", "marketing_start_date": "20220113", "listing_expiration_date": "20261231"}