Package 72572-432-10

Brand: midazolam

Generic: midazolam
NDC Package

Package Facts

Identity

Package NDC 72572-432-10
Digits Only 7257243210
Product NDC 72572-432
Description

10 VIAL in 1 CARTON (72572-432-10) / 5 mL in 1 VIAL (72572-432-01)

Marketing

Marketing Status
Marketed Since 2019-12-10
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": "1b0844b9-17fb-4f81-b438-6fcbb850a0a7", "openfda": {"unii": ["W7TTW573JJ"], "rxcui": ["1666798", "1666800"], "spl_set_id": ["f0c8b6cd-9efc-4344-9212-fbdd3b8e2f9b"], "manufacturer_name": ["Civica, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL in 1 CARTON (72572-432-10)  / 5 mL in 1 VIAL (72572-432-01)", "package_ndc": "72572-432-10", "marketing_start_date": "20191210"}], "brand_name": "Midazolam", "product_id": "72572-432_1b0844b9-17fb-4f81-b438-6fcbb850a0a7", "dosage_form": "INJECTION", "pharm_class": ["Benzodiazepine [EPC]", "Benzodiazepines [CS]"], "product_ndc": "72572-432", "dea_schedule": "CIV", "generic_name": "Midazolam", "labeler_name": "Civica, 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": "20191210", "listing_expiration_date": "20261231"}