Product NDC: | 66312-630 |
Proprietary Name: | Citanest Plain |
Non Proprietary Name: | prilocaine hydrochloride |
Active Ingredient(s): | 40 mg/mL & nbsp; prilocaine hydrochloride |
Administration Route(s): | DENTAL |
Dosage Form(s): | INJECTION, SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 66312-630 |
Labeler Name: | Dentsply Pharmaceutical Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA079235 |
Marketing Category: | ANDA |
Start Marketing Date: | 19651118 |
Package NDC: | 66312-630-14 |
Package Description: | 50 CARTRIDGE in 1 CARTON (66312-630-14) > 1.8 mL in 1 CARTRIDGE |
NDC Code | 66312-630-14 |
Proprietary Name | Citanest Plain |
Package Description | 50 CARTRIDGE in 1 CARTON (66312-630-14) > 1.8 mL in 1 CARTRIDGE |
Product NDC | 66312-630 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | prilocaine hydrochloride |
Dosage Form Name | INJECTION, SOLUTION |
Route Name | DENTAL |
Start Marketing Date | 19651118 |
Marketing Category Name | ANDA |
Labeler Name | Dentsply Pharmaceutical Inc. |
Substance Name | PRILOCAINE HYDROCHLORIDE |
Strength Number | 40 |
Strength Unit | mg/mL |
Pharmaceutical Classes | Amide Local Anesthetic [EPC],Amides [Chemical/Ingredient],Local Anesthesia [PE] |