Product NDC: | 63323-473 |
Proprietary Name: | Sensorcaine |
Non Proprietary Name: | BUPIVACAINE HYDROCHLORIDE |
Active Ingredient(s): | 7.5 mg/mL & nbsp; BUPIVACAINE HYDROCHLORIDE |
Administration Route(s): | SUBARACHNOID |
Dosage Form(s): | INJECTION, SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 63323-473 |
Labeler Name: | APP Pharmaceuticals, LLC |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA071202 |
Marketing Category: | ANDA |
Start Marketing Date: | 20100525 |
Package NDC: | 63323-473-02 |
Package Description: | 10 AMPULE in 1 BOX (63323-473-02) > 2 mL in 1 AMPULE |
NDC Code | 63323-473-02 |
Proprietary Name | Sensorcaine |
Package Description | 10 AMPULE in 1 BOX (63323-473-02) > 2 mL in 1 AMPULE |
Product NDC | 63323-473 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | BUPIVACAINE HYDROCHLORIDE |
Dosage Form Name | INJECTION, SOLUTION |
Route Name | SUBARACHNOID |
Start Marketing Date | 20100525 |
Marketing Category Name | ANDA |
Labeler Name | APP Pharmaceuticals, LLC |
Substance Name | BUPIVACAINE HYDROCHLORIDE |
Strength Number | 7.5 |
Strength Unit | mg/mL |
Pharmaceutical Classes | Amide Local Anesthetic [EPC],Amides [Chemical/Ingredient],Local Anesthesia [PE] |