cisatracurium besylate
- Product NDC
- 0781-9038
- 11-digit product format
- 007819038
- Labeler code
- 0781
- Product ID
- 0781-9038_809e27ca-3d38-4a71-858d-e91d88e3e4a7
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- cisatracurium besylate
- Dosage form
- INJECTION
- Route
- INTRAVENOUS
- Labeler
- Sandoz Inc
- Application
- ANDA200159
- Marketing category
- ANDA
- Marketing start
- 2013-02-28
- Marketing end
- 2021-05-31
- 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
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0781-9038-95 | 00781903895 | 10 VIAL, MULTI-DOSE in 1 CARTON (0781-9038-95) > 10 mL in 1 VIAL, MULTI-DOSE (0781-9038-70) | 2013-02-28 | 2021-05-31 | No | No | Current |