Package 70518-4328-0

Brand: midazolam

Generic: midazolam hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70518-4328-0
Digits Only 7051843280
Product NDC 70518-4328
Product ID 70518-4328_402f646b-1f17-d819-e063-6394a90ab1d8
Description

10 VIAL in 1 CARTON (70518-4328-0) / 2 mL in 1 VIAL (70518-4328-1)

Marketing

Marketing Status
Marketed Since 2025-04-14
Brand midazolam
Generic midazolam hydrochloride
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": "402f646b-1f17-d819-e063-6394a90ab1d8", "openfda": {"unii": ["W7TTW573JJ"], "rxcui": ["1666798"], "spl_set_id": ["d9305142-417d-4d8c-9a23-f9a1b6771cac"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL in 1 CARTON (70518-4328-0)  / 2 mL in 1 VIAL (70518-4328-1)", "package_ndc": "70518-4328-0", "marketing_start_date": "20250414"}], "brand_name": "Midazolam", "product_id": "70518-4328_402f646b-1f17-d819-e063-6394a90ab1d8", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Benzodiazepine [EPC]", "Benzodiazepines [CS]"], "product_ndc": "70518-4328", "dea_schedule": "CIV", "generic_name": "midazolam hydrochloride", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Midazolam", "active_ingredients": [{"name": "MIDAZOLAM HYDROCHLORIDE", "strength": "2 mg/2mL"}], "application_number": "ANDA090315", "marketing_category": "ANDA", "marketing_start_date": "20250414", "listing_expiration_date": "20261231"}