vecuronium bromide

Generic: vecuronium bromide

Labeler: sun pharmaceutical industries, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name vecuronium bromide
Generic Name vecuronium bromide
Labeler sun pharmaceutical industries, inc.
Dosage Form INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Routes
INTRAVENOUS
Active Ingredients

vecuronium bromide 1 mg/mL

Manufacturer
Sun Pharmaceutical Industries, Inc.

Identifiers & Regulatory

Product NDC 47335-932
Product ID 47335-932_82d6bc45-04a5-409a-9223-da1884b2468f
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA079001
Listing Expiration 2026-12-31
Marketing Start 2014-12-15

Pharmacologic Class

Classes
neuromuscular nondepolarizing blockade [pe] nondepolarizing neuromuscular blocker [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 47335932
Hyphenated Format 47335-932

Supplemental Identifiers

RxCUI
859437
UPC
0347335932447
UNII
7E4PHP5N1D

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name vecuronium bromide (source: ndc)
Generic Name vecuronium bromide (source: ndc)
Application Number ANDA079001 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 1 mg/mL
source: ndc
Packaging
  • 10 VIAL in 1 BOX (47335-932-44) / 20 mL in 1 VIAL (47335-932-40)
source: ndc

Packages (1)

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

Ingredients (1)

vecuronium bromide (1 mg/mL)

Linked Drug Pages (1)

vecuronium bromide ndc-match (0.9)

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"}