Rocuronium Bromide
- Product NDC
- 72611-757
- 11-digit product format
- 726110757
- Labeler code
- 72611
- Product ID
- 72611-757_fd1fc286-6525-add9-9e91-52f6972d2128
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- rocuronium bromide
- Dosage form
- INJECTION
- Route
- INTRAVENOUS
- Labeler
- Almaject, Inc.
- Application
- ANDA205656
- Marketing category
- ANDA
- Marketing start
- 2020-03-27
- Marketing end
- 0000-00-00
- Substance
- ROCURONIUM BROMIDE
- Active strength
- 10 mg/mL
- Pharmacologic classes
- Neuromuscular Nondepolarizing Blockade [PE], Nondepolarizing Neuromuscular Blocker [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|
| 72611-757-10 | 72611075710 | 10 VIAL, MULTI-DOSE in 1 CARTON (72611-757-10) > 10 mL in 1 VIAL, MULTI-DOSE (72611-757-01) | 2020-03-27 | 0000-00-00 | No | No | Current |