Package 55150-217-10

Brand: atracurium besylate

Generic: atracurium besylate
NDC Package

Package Facts

Identity

Package NDC 55150-217-10
Digits Only 5515021710
Product NDC 55150-217
Description

10 VIAL, MULTI-DOSE in 1 CARTON (55150-217-10) / 10 mL in 1 VIAL, MULTI-DOSE

Marketing

Marketing Status
Marketed Since 2015-04-08
Brand atracurium besylate
Generic atracurium besylate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "12db80ae-2d05-4941-8c95-8ff454a31d80", "openfda": {"upc": ["0355150217106"], "unii": ["40AX66P76P"], "rxcui": ["966768"], "spl_set_id": ["f7b6a720-05a7-4d6a-9200-21bdc90fc1c4"], "manufacturer_name": ["AuroMedics Pharma LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL, MULTI-DOSE in 1 CARTON (55150-217-10)  / 10 mL in 1 VIAL, MULTI-DOSE", "package_ndc": "55150-217-10", "marketing_start_date": "20150408"}], "brand_name": "Atracurium Besylate", "product_id": "55150-217_12db80ae-2d05-4941-8c95-8ff454a31d80", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Neuromuscular Nondepolarizing Blockade [PE]", "Nondepolarizing Neuromuscular Blocker [EPC]"], "product_ndc": "55150-217", "generic_name": "Atracurium Besylate", "labeler_name": "AuroMedics Pharma LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Atracurium Besylate", "active_ingredients": [{"name": "ATRACURIUM BESYLATE", "strength": "100 mg/10mL"}], "application_number": "ANDA206011", "marketing_category": "ANDA", "marketing_start_date": "20150408", "listing_expiration_date": "20261231"}