Package 25021-661-10

Brand: midazolam

Generic: midazolam hydrochloride
NDC Package

Package Facts

Identity

Package NDC 25021-661-10
Digits Only 2502166110
Product NDC 25021-661
Product ID 25021-661_002ea282-09ba-4d79-8bd1-94c9859f442b
Description

10 VIAL in 1 CARTON (25021-661-10) / 10 mL in 1 VIAL

Marketing

Marketing Status
Marketed Since 2012-03-19
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": "002ea282-09ba-4d79-8bd1-94c9859f442b", "openfda": {"unii": ["W7TTW573JJ"], "rxcui": ["311702"], "spl_set_id": ["880cac48-5c0f-49a9-8aef-3c9770bf5d84"], "manufacturer_name": ["Sagent Pharmaceuticals"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL in 1 CARTON (25021-661-10)  / 10 mL in 1 VIAL", "package_ndc": "25021-661-10", "marketing_start_date": "20120319"}], "brand_name": "midazolam", "product_id": "25021-661_002ea282-09ba-4d79-8bd1-94c9859f442b", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Benzodiazepine [EPC]", "Benzodiazepines [CS]"], "product_ndc": "25021-661", "dea_schedule": "CIV", "generic_name": "midazolam hydrochloride", "labeler_name": "Sagent Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "midazolam", "active_ingredients": [{"name": "MIDAZOLAM HYDROCHLORIDE", "strength": "5 mg/mL"}], "application_number": "ANDA090850", "marketing_category": "ANDA", "marketing_start_date": "20120319", "listing_expiration_date": "20261231"}