Bupivacaine Hydrochloride
- Product NDC
- 71872-7217
- 11-digit product format
- 718727217
- Labeler code
- 71872
- Product ID
- 71872-7217_fad3420b-b53f-f7ae-e053-6294a90a200d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- BUPIVACAINE HYDROCHLORIDE
- Dosage form
- INJECTION, SOLUTION
- Route
- INFILTRATION; PERINEURAL
- Labeler
- Medical Purchasing Solutions, LLC
- Application
- ANDA070590
- Marketing category
- ANDA
- Marketing start
- 2005-04-30
- Substance
- BUPIVACAINE HYDROCHLORIDE
- Active strength
- 2.5 mg/mL
- Pharmacologic classes
- Amide Local Anesthetic [EPC], Amides [CS], Local Anesthesia [PE]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 7TQO7W3VT8 | BUPIVACAINE HYDROCHLORIDE | 73360-54-0 | BUPIVACAINE HYDROCHLORIDE |
Packages
| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 71872-7217-1 | 71872721701 | 1 VIAL, MULTI-DOSE in 1 BAG (71872-7217-1) / 50 mL in 1 VIAL, MULTI-DOSE | 2020-07-16 | No | No | Historical |