Package 72611-741-25

Brand: midazolam

Generic: midazolam
NDC Package

Package Facts

Identity

Package NDC 72611-741-25
Digits Only 7261174125
Product NDC 72611-741
Product ID 72611-741_53563167-5000-bd14-bfa9-a805bc8c200f
Description

25 VIAL, SINGLE-DOSE in 1 CARTON (72611-741-25) / 2 mL in 1 VIAL, SINGLE-DOSE (72611-741-01)

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": "53563167-5000-bd14-bfa9-a805bc8c200f", "openfda": {"upc": ["0372611741253"], "unii": ["W7TTW573JJ"], "rxcui": ["1666798"], "spl_set_id": ["c33919da-1d84-ed01-a5e5-62330407336e"], "manufacturer_name": ["Almaject, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL, SINGLE-DOSE in 1 CARTON (72611-741-25)  / 2 mL in 1 VIAL, SINGLE-DOSE (72611-741-01)", "package_ndc": "72611-741-25", "marketing_end_date": "20260401", "marketing_start_date": "20200414"}], "brand_name": "midazolam", "product_id": "72611-741_53563167-5000-bd14-bfa9-a805bc8c200f", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Benzodiazepine [EPC]", "Benzodiazepines [CS]"], "product_ndc": "72611-741", "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": "1 mg/mL"}], "application_number": "ANDA090696", "marketing_category": "ANDA", "marketing_end_date": "20260401", "marketing_start_date": "20200414"}