Atracurium Besylate
- Product NDC
- 65862-985
- 11-digit product format
- 658620985
- Labeler code
- 65862
- Product ID
- 65862-985_eebbc627-1056-4e18-8f74-7cc4b8f0d6a7
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Atracurium Besylate
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAVENOUS
- Labeler
- Aurobindo Pharma Limited
- Application
- ANDA206011
- Marketing category
- ANDA
- Marketing start
- 2015-04-08
- Marketing end
- 0000-00-00
- Substance
- ATRACURIUM BESYLATE
- Active strength
- 100 mg/10mL
- Pharmacologic classes
- Neuromuscular Nondepolarizing Blockade [PE],Nondepolarizing Neuromuscular Blocker [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record