Package 55150-216-05

Brand: atracurium besylate

Generic: atracurium besylate
NDC Package

Package Facts

Identity

Package NDC 55150-216-05
Digits Only 5515021605
Product NDC 55150-216
Product ID 55150-216_379b43a8-f4ba-4a29-a478-23dbb33fbefa
Description

10 VIAL, SINGLE-USE in 1 CARTON (55150-216-05) / 5 mL in 1 VIAL, SINGLE-USE

Marketing

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

Linked Drug Pages (1)

Atracurium Besylate ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "379b43a8-f4ba-4a29-a478-23dbb33fbefa", "openfda": {"unii": ["40AX66P76P"], "rxcui": ["1718913"], "spl_set_id": ["71d4bc78-57df-474b-8b19-811a959f1fce"], "manufacturer_name": ["AuroMedics Pharma LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL, SINGLE-USE in 1 CARTON (55150-216-05)  / 5 mL in 1 VIAL, SINGLE-USE", "package_ndc": "55150-216-05", "marketing_start_date": "20150408"}], "brand_name": "Atracurium Besylate", "product_id": "55150-216_379b43a8-f4ba-4a29-a478-23dbb33fbefa", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Neuromuscular Nondepolarizing Blockade [PE]", "Nondepolarizing Neuromuscular Blocker [EPC]"], "product_ndc": "55150-216", "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": "50 mg/5mL"}], "application_number": "ANDA206010", "marketing_category": "ANDA", "marketing_start_date": "20150408", "listing_expiration_date": "20261231"}