Package 0409-0001-25

Brand: midazolam

Generic: midazolam hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0409-0001-25
Digits Only 0409000125
Product NDC 0409-0001
Description

25 VIAL, SINGLE-DOSE in 1 CARTON (0409-0001-25) / 2 mL in 1 VIAL, SINGLE-DOSE (0409-0001-01)

Marketing

Marketing Status
Marketed Since 2025-01-27
Brand midazolam
Generic midazolam hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "8c3cf34b-901d-407a-946d-a1556bb24551", "openfda": {"unii": ["W7TTW573JJ"], "rxcui": ["1666798", "1666800", "1666814", "1666823"], "spl_set_id": ["1abda8b8-48a8-4995-af86-39220d1aa240"], "manufacturer_name": ["Hospira, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL, SINGLE-DOSE in 1 CARTON (0409-0001-25)  / 2 mL in 1 VIAL, SINGLE-DOSE (0409-0001-01)", "package_ndc": "0409-0001-25", "marketing_start_date": "20250127"}], "brand_name": "Midazolam", "product_id": "0409-0001_8c3cf34b-901d-407a-946d-a1556bb24551", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Benzodiazepine [EPC]", "Benzodiazepines [CS]"], "product_ndc": "0409-0001", "dea_schedule": "CIV", "generic_name": "MIDAZOLAM HYDROCHLORIDE", "labeler_name": "Hospira, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Midazolam", "active_ingredients": [{"name": "MIDAZOLAM HYDROCHLORIDE", "strength": "1 mg/mL"}], "application_number": "ANDA075857", "marketing_category": "ANDA", "marketing_start_date": "20250127", "listing_expiration_date": "20261231"}