Cisatracurium Besylate
- Product NDC
- 23155-768
- 11-digit product format
- 231550768
- Labeler code
- 23155
- Product ID
- 23155-768_712e7133-088a-49ae-badb-d5caeebe02b4
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Cisatracurium Besylate
- Dosage form
- INJECTION
- Route
- INTRAVENOUS
- Labeler
- Avet Pharmaceuticals Inc.
- Application
- ANDA212190
- Marketing category
- ANDA
- Marketing start
- 2020-10-04
- Marketing end
- 0000-00-00
- Substance
- CISATRACURIUM BESYLATE
- Active strength
- 2 mg/mL
- Pharmacologic classes
- Neuromuscular Nondepolarizing Blockade [PE],Nondepolarizing Neuromuscular Blocker [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- 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 |
|---|
| 23155-768-41 | 23155076841 | 10 CARTON in 1 CARTON (23155-768-41) > 1 VIAL, MULTI-DOSE in 1 CARTON (23155-768-31) > 10 mL in 1 VIAL, MULTI-DOSE | 10 carton | 2020-10-04 | 0000-00-00 | No | No | Current |