Package 0143-9379-10

Brand: midazolam in sodium chloride

Generic: midazolam in sodium chloride
NDC Package

Package Facts

Identity

Package NDC 0143-9379-10
Digits Only 0143937910
Product NDC 0143-9379
Description

10 POUCH in 1 CARTON (0143-9379-10) / 1 BAG in 1 POUCH (0143-9379-01) / 50 mL in 1 BAG

Marketing

Marketing Status
Marketed Since 2023-05-19
Brand midazolam in sodium chloride
Generic midazolam in sodium chloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "a6be32fe-dc3d-4ce0-b780-8ba6b4261acc", "openfda": {"unii": ["W7TTW573JJ"], "rxcui": ["2541170", "2541171"], "spl_set_id": ["4155a60a-b023-4f4a-acae-7bb8fe9dc0c1"], "manufacturer_name": ["Hikma Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 POUCH in 1 CARTON (0143-9379-10)  / 1 BAG in 1 POUCH (0143-9379-01)  / 50 mL in 1 BAG", "package_ndc": "0143-9379-10", "marketing_start_date": "20230519"}], "brand_name": "Midazolam in Sodium Chloride", "product_id": "0143-9379_a6be32fe-dc3d-4ce0-b780-8ba6b4261acc", "dosage_form": "INJECTION", "pharm_class": ["Benzodiazepine [EPC]", "Benzodiazepines [CS]"], "product_ndc": "0143-9379", "dea_schedule": "CIV", "generic_name": "Midazolam in Sodium Chloride", "labeler_name": "Hikma Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Midazolam in Sodium Chloride", "active_ingredients": [{"name": "MIDAZOLAM HYDROCHLORIDE", "strength": "1 mg/mL"}], "application_number": "ANDA216159", "marketing_category": "ANDA", "marketing_start_date": "20230519", "listing_expiration_date": "20261231"}