Package 0781-3152-95
Brand: cisatracurium besylate
Generic: cisatracurium besylatePackage Facts
Identity
Package NDC
0781-3152-95
Digits Only
0781315295
Product NDC
0781-3152
Description
10 VIAL, MULTI-DOSE in 1 CARTON (0781-3152-95) / 10 mL in 1 VIAL, MULTI-DOSE (0781-3152-70)
Marketing
Marketing Status
Brand
cisatracurium besylate
Generic
cisatracurium besylate
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "bb1408b3-f751-45cd-84c9-3e5bff7dbdd0", "openfda": {"unii": ["80YS8O1MBS"], "rxcui": ["199211"], "spl_set_id": ["2ee0358e-2cce-40d3-9fcf-1b9088815c98"], "manufacturer_name": ["Sandoz Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL, MULTI-DOSE in 1 CARTON (0781-3152-95) / 10 mL in 1 VIAL, MULTI-DOSE (0781-3152-70)", "package_ndc": "0781-3152-95", "marketing_start_date": "20120716"}], "brand_name": "cisatracurium besylate", "product_id": "0781-3152_bb1408b3-f751-45cd-84c9-3e5bff7dbdd0", "dosage_form": "INJECTION", "pharm_class": ["Neuromuscular Nondepolarizing Blockade [PE]", "Nondepolarizing Neuromuscular Blocker [EPC]"], "product_ndc": "0781-3152", "generic_name": "cisatracurium besylate", "labeler_name": "Sandoz Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "cisatracurium besylate", "active_ingredients": [{"name": "CISATRACURIUM BESYLATE", "strength": "2 mg/mL"}], "application_number": "ANDA200159", "marketing_category": "ANDA", "marketing_start_date": "20120716", "listing_expiration_date": "20261231"}