Rocuronium Bromide
- Product NDC
- 71872-7211
- 11-digit product format
- 718727211
- Labeler code
- 71872
- Product ID
- 71872-7211_ada262ed-bac5-28c7-e053-2a95a90aed5f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- rocuronium bromide
- Dosage form
- INJECTION
- Route
- INTRAVENOUS
- Labeler
- Medical Purchasing Solutions, LLC
- Application
- ANDA205656
- Marketing category
- ANDA
- Marketing start
- 2018-04-27
- 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
- 2021-12-31
- 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 |
|---|
| 71872-7211-1 | 71872721101 | 1 VIAL, MULTI-DOSE in 1 BAG (71872-7211-1) > 5 mL in 1 VIAL, MULTI-DOSE | 2020-04-07 | 0000-00-00 | No | No | Current |