Bupivacaine Hydrochloride
- Product NDC
- 36000-092
- 11-digit product format
- 360000092
- Labeler code
- 36000
- Product ID
- 36000-092_5d4f1648-9e05-4d0a-81cc-581897036cc7
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- BUPIVACAINE HYDROCHLORIDE
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRASPINAL
- Labeler
- Baxter Healthcare Corporation
- Application
- ANDA207266
- Marketing category
- ANDA
- Marketing start
- 2016-08-08
- Marketing end
- 0000-00-00
- Substance
- BUPIVACAINE HYDROCHLORIDE
- Active strength
- 8 mg/mL
- Pharmacologic classes
- Amide Local Anesthetic [EPC], Amides [CS], Local Anesthesia [PE]
- 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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 36000-092-10 | 36000009210 | 10 AMPULE in 1 BLISTER PACK (36000-092-10) > 2 mL in 1 AMPULE | 10 ampule | 2016-08-08 | 0000-00-00 | No | No | Current |