Atracurium Besylate
- Product NDC
- 67457-698
- 11-digit product format
- 674570698
- Labeler code
- 67457
- Product ID
- 67457-698_5be0df06-6aeb-4e52-af83-2667f509b0ad
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- atracurium besylate
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAVENOUS
- Labeler
- Mylan Institutional LLC
- Application
- ANDA206096
- 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