atracurium besylate
Generic: atracurium besylate
Labeler: meitheal pharmaceuticals inc.Drug Facts
Product Profile
Brand Name
atracurium besylate
Generic Name
atracurium besylate
Labeler
meitheal pharmaceuticals inc.
Dosage Form
INJECTION, SOLUTION
Routes
Active Ingredients
atracurium besylate 10 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
71288-702
Product ID
71288-702_2e0da959-ece2-4643-9b93-a1ce7d59efdd
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA091489
Listing Expiration
2026-12-31
Marketing Start
2018-05-15
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
71288702
Hyphenated Format
71288-702
Supplemental Identifiers
RxCUI
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
ANDA091489 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 10 mg/mL
Packaging
- 10 VIAL, MULTI-DOSE in 1 CARTON (71288-702-10) / 10 mL in 1 VIAL, MULTI-DOSE (71288-702-11)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "2e0da959-ece2-4643-9b93-a1ce7d59efdd", "openfda": {"unii": ["40AX66P76P"], "rxcui": ["966768", "1718913"], "spl_set_id": ["efe90ee2-fe9e-421f-9e54-2961085d3b12"], "manufacturer_name": ["Meitheal Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL, MULTI-DOSE in 1 CARTON (71288-702-10) / 10 mL in 1 VIAL, MULTI-DOSE (71288-702-11)", "package_ndc": "71288-702-10", "marketing_start_date": "20180515"}], "brand_name": "Atracurium Besylate", "product_id": "71288-702_2e0da959-ece2-4643-9b93-a1ce7d59efdd", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Neuromuscular Nondepolarizing Blockade [PE]", "Nondepolarizing Neuromuscular Blocker [EPC]"], "product_ndc": "71288-702", "generic_name": "Atracurium Besylate", "labeler_name": "Meitheal Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Atracurium Besylate", "active_ingredients": [{"name": "ATRACURIUM BESYLATE", "strength": "10 mg/mL"}], "application_number": "ANDA091489", "marketing_category": "ANDA", "marketing_start_date": "20180515", "listing_expiration_date": "20261231"}