Product NDC: | 52584-160 |
Proprietary Name: | Bupivacaine Hydrochloride |
Non Proprietary Name: | Bupivacaine Hydrochloride |
Active Ingredient(s): | 2.5 mg/mL & nbsp; Bupivacaine Hydrochloride |
Administration Route(s): | INFILTRATION |
Dosage Form(s): | INJECTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 52584-160 |
Labeler Name: | General Injectables & Vaccines, Inc |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA070590 |
Marketing Category: | ANDA |
Start Marketing Date: | 20100701 |
Package NDC: | 52584-160-01 |
Package Description: | 1 VIAL, MULTI-DOSE in 1 BAG (52584-160-01) > 50 mL in 1 VIAL, MULTI-DOSE |
NDC Code | 52584-160-01 |
Proprietary Name | Bupivacaine Hydrochloride |
Package Description | 1 VIAL, MULTI-DOSE in 1 BAG (52584-160-01) > 50 mL in 1 VIAL, MULTI-DOSE |
Product NDC | 52584-160 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Bupivacaine Hydrochloride |
Dosage Form Name | INJECTION |
Route Name | INFILTRATION |
Start Marketing Date | 20100701 |
Marketing Category Name | ANDA |
Labeler Name | General Injectables & Vaccines, Inc |
Substance Name | BUPIVACAINE HYDROCHLORIDE |
Strength Number | 2.5 |
Strength Unit | mg/mL |
Pharmaceutical Classes | Amide Local Anesthetic [EPC],Amides [Chemical/Ingredient],Local Anesthesia [PE] |