cisatracurium besylate
- Product NDC
- 72572-067
- 11-digit product format
- 725720067
- Labeler code
- 72572
- Product ID
- 72572-067_887171ff-1f2f-4115-90a9-39d05cd5b955
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- cisatracurium besylate
- Dosage form
- INJECTION
- Route
- INTRAVENOUS
- Labeler
- Civica, Inc.
- Application
- ANDA200154
- Marketing category
- ANDA
- Marketing start
- 2022-12-21
- 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
- 2024-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 72572-067-10 | 72572006710 | 10 BOX in 1 CARTON (72572-067-10) > 1 VIAL in 1 BOX (72572-067-01) > 20 mL in 1 VIAL | 10 box | 2022-12-21 | 0000-00-00 | No | No | Current |