atracurium besylate

Generic: atracurium besylate

Labeler: auromedics pharma llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name atracurium besylate
Generic Name atracurium besylate
Labeler auromedics pharma llc
Dosage Form INJECTION, SOLUTION
Routes
INTRAVENOUS
Active Ingredients

atracurium besylate 50 mg/5mL

Manufacturer
AuroMedics Pharma LLC

Identifiers & Regulatory

Product NDC 55150-216
Product ID 55150-216_379b43a8-f4ba-4a29-a478-23dbb33fbefa
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA206010
Listing Expiration 2026-12-31
Marketing Start 2015-04-08

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 55150216
Hyphenated Format 55150-216

Supplemental Identifiers

RxCUI
1718913
UNII
40AX66P76P

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 atracurium besylate (source: ndc)
Generic Name atracurium besylate (source: ndc)
Application Number ANDA206010 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 50 mg/5mL
source: ndc
Packaging
  • 10 VIAL, SINGLE-USE in 1 CARTON (55150-216-05) / 5 mL in 1 VIAL, SINGLE-USE
source: ndc

Packages (1)

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

Ingredients (1)

atracurium besylate (50 mg/5mL)

Linked Drug Pages (1)

Atracurium Besylate ndc-match (0.9)

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"}