Bupivacaine Hydrochloride
- Product NDC
- 70518-2360
- 11-digit product format
- 705182360
- Labeler code
- 70518
- Product ID
- 70518-2360_c894a720-ef94-58ff-e053-2995a90aae37
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Bupivacaine Hydrochloride
- Dosage form
- INJECTION, SOLUTION
- Route
- EPIDURAL; INTRACAUDAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA203895
- Marketing category
- ANDA
- Marketing start
- 2019-10-10
- Marketing end
- 0000-00-00
- Substance
- BUPIVACAINE HYDROCHLORIDE
- Active strength
- 5 mg/mL
- Pharmacologic classes
- Amide Local Anesthetic [EPC],Amides [CS],Local Anesthesia [PE]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- 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 |
|---|
| 70518-2360-0 | 70518236000 | 25 VIAL, SINGLE-DOSE in 1 CARTON (70518-2360-0) > 10 mL in 1 VIAL, SINGLE-DOSE (70518-2360-1) | 2019-10-10 | 0000-00-00 | No | No | Current |