Package 47335-932-44

Brand: vecuronium bromide

Generic: vecuronium bromide
NDC Package

Package Facts

Identity

Package NDC 47335-932-44
Digits Only 4733593244
Product NDC 47335-932
Description

10 VIAL in 1 BOX (47335-932-44) / 20 mL in 1 VIAL (47335-932-40)

Marketing

Marketing Status
Marketed Since 2014-12-15
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": "82d6bc45-04a5-409a-9223-da1884b2468f", "openfda": {"upc": ["0347335932447"], "unii": ["7E4PHP5N1D"], "rxcui": ["859437"], "spl_set_id": ["a14da3ee-a731-4282-be9d-407473517470"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL in 1 BOX (47335-932-44)  / 20 mL in 1 VIAL (47335-932-40)", "package_ndc": "47335-932-44", "marketing_start_date": "20141215"}], "brand_name": "vecuronium bromide", "product_id": "47335-932_82d6bc45-04a5-409a-9223-da1884b2468f", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Neuromuscular Nondepolarizing Blockade [PE]", "Nondepolarizing Neuromuscular Blocker [EPC]"], "product_ndc": "47335-932", "generic_name": "vecuronium bromide", "labeler_name": "Sun Pharmaceutical Industries, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "vecuronium bromide", "active_ingredients": [{"name": "VECURONIUM BROMIDE", "strength": "1 mg/mL"}], "application_number": "ANDA079001", "marketing_category": "ANDA", "marketing_start_date": "20141215", "listing_expiration_date": "20261231"}