Rocuronium Bromide
- Product NDC
- 70860-651
- 11-digit product format
- 708600651
- Labeler code
- 70860
- Product ID
- 70860-651_3675d526-7969-4e02-ba44-0a7216ee9651
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- rocuronium bromide
- Dosage form
- SOLUTION
- Route
- INTRAVENOUS
- Labeler
- Athenex Pharmaceutical Division, LLC.
- Application
- ANDA205656
- Marketing category
- ANDA
- Marketing start
- 2018-06-15
- 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
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70860-651-05 | 70860065105 | 10 VIAL, MULTI-DOSE in 1 CARTON (70860-651-05) > 5 mL in 1 VIAL, MULTI-DOSE (70860-651-41) | 2018-06-15 | 0000-00-00 | No | No | Current |
| 70860-651-10 | 70860065110 | 10 VIAL, MULTI-DOSE in 1 CARTON (70860-651-10) > 10 mL in 1 VIAL, MULTI-DOSE (70860-651-42) | 2018-06-15 | 0000-00-00 | No | No | Current |