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Polocaine
Polocaine - 63323-296-50 - (MEPIVACAINE HYDROCHLORIDE)
Drug Information of Polocaine
| Product NDC: | 63323-296 |
| Proprietary Name: | Polocaine |
| Non Proprietary Name: | MEPIVACAINE HYDROCHLORIDE |
| Active Ingredient(s): | 20 mg/mL & nbsp; MEPIVACAINE HYDROCHLORIDE |
| Administration Route(s): | INFILTRATION |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Polocaine
| Product NDC: | 63323-296 |
| Labeler Name: | APP Pharmaceuticals, LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA089410 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20090720 |
Package Information of Polocaine
| Package NDC: | 63323-296-50 |
| Package Description: | 1 VIAL in 1 BOX (63323-296-50) > 50 mL in 1 VIAL |
NDC Information of Polocaine
| NDC Code | 63323-296-50 |
| Proprietary Name | Polocaine |
| Package Description | 1 VIAL in 1 BOX (63323-296-50) > 50 mL in 1 VIAL |
| Product NDC | 63323-296 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | MEPIVACAINE HYDROCHLORIDE |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INFILTRATION |
| Start Marketing Date | 20090720 |
| Marketing Category Name | ANDA |
| Labeler Name | APP Pharmaceuticals, LLC |
| Substance Name | MEPIVACAINE HYDROCHLORIDE |
| Strength Number | 20 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Amide Local Anesthetic [EPC],Amides [Chemical/Ingredient],Local Anesthesia [PE] |
