ROCURONIUM BROMIDE
- Product NDC
- 51662-1545
- 11-digit product format
- 516621545
- Labeler code
- 51662
- Product ID
- 51662-1545_dc444a4b-16eb-568d-e053-2995a90a53a7
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- ROCURONIUM BROMIDE
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAVENOUS
- Labeler
- HF Acquisition Co LLC, DBA HealthFirst
- Application
- ANDA206206
- Marketing category
- ANDA
- Marketing start
- 2022-04-09
- Substance
- ROCURONIUM BROMIDE
- Active strength
- 100 mg/10mL
- Pharmacologic classes
- Neuromuscular Nondepolarizing Blockade [PE], Nondepolarizing Neuromuscular Blocker [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| I65MW4OFHZ | ROCURONIUM BROMIDE | 119302-91-9 | ROCURONIUM BROMIDE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 51662-1545-1 | 51662154501 | 10 mL in 1 VIAL, MULTI-DOSE (51662-1545-1) | 10 ml | 2022-04-09 | No | No | Historical |