atracurium besylate
Generic: atracurium besylate
Labeler: auromedics pharma llcDrug Facts
Product Profile
Brand Name
atracurium besylate
Generic Name
atracurium besylate
Labeler
auromedics pharma llc
Dosage Form
INJECTION, SOLUTION
Routes
Active Ingredients
atracurium besylate 100 mg/10mL
Manufacturer
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
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
55150217
Hyphenated Format
55150-217
Supplemental Identifiers
RxCUI
UPC
UNII
Packaging Origin
Original Packager
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
source: ndc
Resolved Composition
Strengths
- 100 mg/10mL
Packaging
- 10 VIAL, MULTI-DOSE in 1 CARTON (55150-217-10) / 10 mL in 1 VIAL, MULTI-DOSE
Packages (1)
Ingredients (1)
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"}