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 100 mg/10mL

Manufacturer
AuroMedics Pharma LLC

Identifiers & Regulatory

Product NDC 55150-217
Product ID 55150-217_12db80ae-2d05-4941-8c95-8ff454a31d80
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA206011
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 55150217
Hyphenated Format 55150-217

Supplemental Identifiers

RxCUI
966768
UPC
0355150217106
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 ANDA206011 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 100 mg/10mL
source: ndc
Packaging
  • 10 VIAL, MULTI-DOSE in 1 CARTON (55150-217-10) / 10 mL in 1 VIAL, MULTI-DOSE
source: ndc

Packages (1)

Ingredients (1)

atracurium besylate (100 mg/10mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "12db80ae-2d05-4941-8c95-8ff454a31d80", "openfda": {"upc": ["0355150217106"], "unii": ["40AX66P76P"], "rxcui": ["966768"], "spl_set_id": ["f7b6a720-05a7-4d6a-9200-21bdc90fc1c4"], "manufacturer_name": ["AuroMedics Pharma LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL, MULTI-DOSE in 1 CARTON (55150-217-10)  / 10 mL in 1 VIAL, MULTI-DOSE", "package_ndc": "55150-217-10", "marketing_start_date": "20150408"}], "brand_name": "Atracurium Besylate", "product_id": "55150-217_12db80ae-2d05-4941-8c95-8ff454a31d80", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Neuromuscular Nondepolarizing Blockade [PE]", "Nondepolarizing Neuromuscular Blocker [EPC]"], "product_ndc": "55150-217", "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": "100 mg/10mL"}], "application_number": "ANDA206011", "marketing_category": "ANDA", "marketing_start_date": "20150408", "listing_expiration_date": "20261231"}