Home
>
National Drug Code (NDC)
>
Nesacaine
Nesacaine - 63323-476-37 - (CHLOROPROCAINE HYDROCHLORIDE)
Drug Information of Nesacaine
| Product NDC: | 63323-476 |
| 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: | 63323-476 |
| Labeler Name: | APP Pharmaceuticals, LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA009435 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20101014 |
Package Information of Nesacaine
| Package NDC: | 63323-476-37 |
| Package Description: | 25 VIAL, MULTI-DOSE in 1 CARTON (63323-476-37) > 30 mL in 1 VIAL, MULTI-DOSE |
NDC Information of Nesacaine
| NDC Code | 63323-476-37 |
| Proprietary Name | Nesacaine |
| Package Description | 25 VIAL, MULTI-DOSE in 1 CARTON (63323-476-37) > 30 mL in 1 VIAL, MULTI-DOSE |
| Product NDC | 63323-476 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | CHLOROPROCAINE HYDROCHLORIDE |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INFILTRATION; PERINEURAL |
| Start Marketing Date | 20101014 |
| Marketing Category Name | NDA |
| Labeler Name | APP Pharmaceuticals, LLC |
| Substance Name | CHLOROPROCAINE HYDROCHLORIDE |
| Strength Number | 20 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Ester Local Anesthetic [EPC],Esters [Chemical/Ingredient],Local Anesthesia [PE] |
