Package 0404-9915-05

Brand: midazolam

Generic: midazolam
NDC Package

Package Facts

Identity

Package NDC 0404-9915-05
Digits Only 0404991505
Product NDC 0404-9915
Description

1 VIAL in 1 BAG (0404-9915-05) / 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": "69f7e7ff-2ac4-4df5-8c26-6e5eb13783f5", "openfda": {"unii": ["W7TTW573JJ"], "rxcui": ["311702"], "spl_set_id": ["90f7b7f6-d0fd-40af-bbfa-70b152e3e27c"], "manufacturer_name": ["Henry Schein, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 BAG (0404-9915-05)  / 5 mL in 1 VIAL", "package_ndc": "0404-9915-05", "marketing_start_date": "20220113"}], "brand_name": "Midazolam", "product_id": "0404-9915_69f7e7ff-2ac4-4df5-8c26-6e5eb13783f5", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Benzodiazepine [EPC]", "Benzodiazepines [CS]"], "product_ndc": "0404-9915", "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": "5 mg/mL"}], "application_number": "ANDA075293", "marketing_category": "ANDA", "marketing_start_date": "20220113", "listing_expiration_date": "20261231"}