Product NDC: | 63323-464 |
Proprietary Name: | SENSORCAINE |
Non Proprietary Name: | BUPIVACAINE HYDROCHLORIDE |
Active Ingredient(s): | 2.5 mg/mL & nbsp; BUPIVACAINE HYDROCHLORIDE |
Administration Route(s): | EPIDURAL; INFILTRATION; INTRACAUDAL; PERINEURAL |
Dosage Form(s): | INJECTION, SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 63323-464 |
Labeler Name: | APP Pharmaceuticals, LLC |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA018304 |
Marketing Category: | ANDA |
Start Marketing Date: | 20101119 |
Package NDC: | 63323-464-33 |
Package Description: | 5 AMPULE in 1 BOX (63323-464-33) > 30 mL in 1 AMPULE |
NDC Code | 63323-464-33 |
Proprietary Name | SENSORCAINE |
Package Description | 5 AMPULE in 1 BOX (63323-464-33) > 30 mL in 1 AMPULE |
Product NDC | 63323-464 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | BUPIVACAINE HYDROCHLORIDE |
Dosage Form Name | INJECTION, SOLUTION |
Route Name | EPIDURAL; INFILTRATION; INTRACAUDAL; PERINEURAL |
Start Marketing Date | 20101119 |
Marketing Category Name | ANDA |
Labeler Name | APP Pharmaceuticals, LLC |
Substance Name | BUPIVACAINE HYDROCHLORIDE |
Strength Number | 2.5 |
Strength Unit | mg/mL |
Pharmaceutical Classes | Amide Local Anesthetic [EPC],Amides [Chemical/Ingredient],Local Anesthesia [PE] |