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NESACAINE
NESACAINE - 52584-476-37 - (chloroprocaine hydrochloride)
Drug Information of NESACAINE
| Product NDC: | 52584-476 |
| Proprietary Name: | NESACAINE |
| Non Proprietary Name: | chloroprocaine hydrochloride |
| Active Ingredient(s): | 20 mg/mL & nbsp; chloroprocaine hydrochloride |
| Administration Route(s): | INFILTRATION; PERINEURAL |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of NESACAINE
| Product NDC: | 52584-476 |
| Labeler Name: | General Injectables & Vaccines, Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA009435 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20130130 |
Package Information of NESACAINE
| Package NDC: | 52584-476-37 |
| Package Description: | 1 VIAL, MULTI-DOSE in 1 BAG (52584-476-37) > 30 mL in 1 VIAL, MULTI-DOSE |
NDC Information of NESACAINE
| NDC Code | 52584-476-37 |
| Proprietary Name | NESACAINE |
| Package Description | 1 VIAL, MULTI-DOSE in 1 BAG (52584-476-37) > 30 mL in 1 VIAL, MULTI-DOSE |
| Product NDC | 52584-476 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | chloroprocaine hydrochloride |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INFILTRATION; PERINEURAL |
| Start Marketing Date | 20130130 |
| Marketing Category Name | NDA |
| Labeler Name | General Injectables & Vaccines, Inc |
| Substance Name | CHLOROPROCAINE HYDROCHLORIDE |
| Strength Number | 20 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Ester Local Anesthetic [EPC],Esters [Chemical/Ingredient],Local Anesthesia [PE] |
