Package 63323-781-44

Brand: vecuronium bromide

Generic: vecuronium bromide
NDC Package

Package Facts

Identity

Package NDC 63323-781-44
Digits Only 6332378144
Product NDC 63323-781
Description

10 VIAL in 1 CARTON (63323-781-44) / 10 mL in 1 VIAL (63323-781-41)

Marketing

Marketing Status
Marketed Since 2016-06-30
Brand vecuronium bromide
Generic vecuronium bromide
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "19b712c5-7fb2-435c-aa19-6e63fd1ced39", "openfda": {"unii": ["7E4PHP5N1D"], "rxcui": ["859437"], "spl_set_id": ["f3c304f8-de85-4b35-9644-0928b370827f"], "manufacturer_name": ["Fresenius Kabi USA, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL in 1 CARTON (63323-781-44)  / 10 mL in 1 VIAL (63323-781-41)", "package_ndc": "63323-781-44", "marketing_start_date": "20160630"}], "brand_name": "Vecuronium Bromide", "product_id": "63323-781_19b712c5-7fb2-435c-aa19-6e63fd1ced39", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Neuromuscular Nondepolarizing Blockade [PE]", "Nondepolarizing Neuromuscular Blocker [EPC]"], "product_ndc": "63323-781", "generic_name": "Vecuronium Bromide", "labeler_name": "Fresenius Kabi USA, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Vecuronium Bromide", "active_ingredients": [{"name": "VECURONIUM BROMIDE", "strength": "1 mg/mL"}], "application_number": "ANDA205390", "marketing_category": "ANDA", "marketing_start_date": "20160630", "listing_expiration_date": "20261231"}