Atracurium Besylate

Product NDC
67457-699
11-digit product format
674570699
Labeler code
67457
Product ID
67457-699_cb4fcc57-6b2e-4ab5-84a4-217d9fa4910d
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
atracurium besylate
Dosage form
INJECTION, SOLUTION
Route
INTRAVENOUS
Labeler
Mylan Institutional LLC
Application
ANDA206001
Marketing category
ANDA
Marketing start
2017-10-19
Marketing end
2019-08-31
Substance
ATRACURIUM BESYLATE
Active strength
10 mg/mL
Pharmacologic classes
Neuromuscular Nondepolarizing Blockade [PE],Nondepolarizing Neuromuscular Blocker [EPC]
NDC exclude flag
No
Listing certified through
0000-00-00
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
67457-699-00ML - Milliliter67457-6997bcb0d9e-c2b1-4d03-a8ee-aa7f9e15b93612017-11-06
67457-699-05ML - Milliliter67457-699c94be502-53fc-47ea-9b88-c0f12fe81cdc12017-11-06