Package 72611-749-10

Brand: midazolam

Generic: midazolam
NDC Package

Package Facts

Identity

Package NDC 72611-749-10
Digits Only 7261174910
Product NDC 72611-749
Product ID 72611-749_511292f9-41d1-96c6-6fa9-0c00078b7ae1
Description

10 VIAL, MULTI-DOSE in 1 CARTON (72611-749-10) / 10 mL in 1 VIAL, MULTI-DOSE (72611-749-01)

Marketing

Marketing Status
Discontinued 2026-04-01
Brand midazolam
Generic midazolam
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": "511292f9-41d1-96c6-6fa9-0c00078b7ae1", "openfda": {"upc": ["0372611749105"], "unii": ["W7TTW573JJ"], "rxcui": ["311702"], "spl_set_id": ["9532689f-bf0f-5854-98ef-543a0ae2d8c8"], "manufacturer_name": ["Almaject, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL, MULTI-DOSE in 1 CARTON (72611-749-10)  / 10 mL in 1 VIAL, MULTI-DOSE (72611-749-01)", "package_ndc": "72611-749-10", "marketing_end_date": "20260401", "marketing_start_date": "20200414"}], "brand_name": "midazolam", "product_id": "72611-749_511292f9-41d1-96c6-6fa9-0c00078b7ae1", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Benzodiazepine [EPC]", "Benzodiazepines [CS]"], "product_ndc": "72611-749", "dea_schedule": "CIV", "generic_name": "midazolam", "labeler_name": "Almaject, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "midazolam", "active_ingredients": [{"name": "MIDAZOLAM HYDROCHLORIDE", "strength": "5 mg/mL"}], "application_number": "ANDA090850", "marketing_category": "ANDA", "marketing_end_date": "20260401", "marketing_start_date": "20200414"}