Package 70069-818-10

Brand: midazolam

Generic: midazolam hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70069-818-10
Digits Only 7006981810
Product NDC 70069-818
Product ID 70069-818_0bbe7c1c-5228-e584-e063-6294a90ad750
Description

10 VIAL in 1 CARTON (70069-818-10) / 10 mL in 1 VIAL

Marketing

Marketing Status
Marketed Since 2023-12-05
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": "0bbe7c1c-5228-e584-e063-6294a90ad750", "openfda": {"upc": ["0370069818015"], "unii": ["W7TTW573JJ"], "rxcui": ["311702"], "spl_set_id": ["06e4f754-72df-4eb4-aaed-b538524f5277"], "manufacturer_name": ["SOMERSET THERAPEUTICS, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL in 1 CARTON (70069-818-10)  / 10 mL in 1 VIAL", "package_ndc": "70069-818-10", "marketing_start_date": "20231205"}], "brand_name": "Midazolam", "product_id": "70069-818_0bbe7c1c-5228-e584-e063-6294a90ad750", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Benzodiazepine [EPC]", "Benzodiazepines [CS]"], "product_ndc": "70069-818", "dea_schedule": "CIV", "generic_name": "midazolam hydrochloride", "labeler_name": "SOMERSET THERAPEUTICS, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Midazolam", "active_ingredients": [{"name": "MIDAZOLAM HYDROCHLORIDE", "strength": "5 mg/mL"}], "application_number": "ANDA090316", "marketing_category": "ANDA", "marketing_start_date": "20231205", "listing_expiration_date": "20261231"}