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SENSORCAINE
SENSORCAINE - 63323-472-37 - (BUPIVACAINE HYDROCHLORIDE)
Drug Information of SENSORCAINE
| Product NDC: | 63323-472 |
| Proprietary Name: | SENSORCAINE |
| Non Proprietary Name: | BUPIVACAINE HYDROCHLORIDE |
| Active Ingredient(s): | 7.5 mg/mL & nbsp; BUPIVACAINE HYDROCHLORIDE |
| Administration Route(s): | EPIDURAL; RETROBULBAR |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of SENSORCAINE
| Product NDC: | 63323-472 |
| Labeler Name: | APP Pharmaceuticals, LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA070554 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20101119 |
Package Information of SENSORCAINE
| Package NDC: | 63323-472-37 |
| Package Description: | 25 VIAL, SINGLE-DOSE in 1 CARTON (63323-472-37) > 30 mL in 1 VIAL, SINGLE-DOSE |
NDC Information of SENSORCAINE
| NDC Code | 63323-472-37 |
| Proprietary Name | SENSORCAINE |
| Package Description | 25 VIAL, SINGLE-DOSE in 1 CARTON (63323-472-37) > 30 mL in 1 VIAL, SINGLE-DOSE |
| Product NDC | 63323-472 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | BUPIVACAINE HYDROCHLORIDE |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | EPIDURAL; RETROBULBAR |
| Start Marketing Date | 20101119 |
| 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] |
