CISATRACURIUM BESYLATE
- Product NDC
- 57884-3063
- 11-digit product format
- 578843063
- Labeler code
- 57884
- Product ID
- 57884-3063_7f34a8ee-1ad6-816a-e053-2991aa0aa7c4
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Cisatracurium besylate
- Dosage form
- INJECTION
- Route
- INTRAVENOUS
- Labeler
- Jiangsu Hengrui Medicine Co., Ltd.
- Application
- ANDA204960
- Marketing category
- ANDA
- Marketing start
- 2017-09-19
- Marketing end
- 0000-00-00
- Substance
- CISATRACURIUM BESYLATE
- Active strength
- 10 mg/mL
- Pharmacologic classes
- Neuromuscular Nondepolarizing Blockade [PE],Nondepolarizing Neuromuscular Blocker [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record