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Citanest Forte
Citanest Forte - 66312-540-16 - (prilocaine hydrochloride and epinephrine bitartrate)
Drug Information of Citanest Forte
| Product NDC: | 66312-540 |
| Proprietary Name: | Citanest Forte |
| Non Proprietary Name: | prilocaine hydrochloride and epinephrine bitartrate |
| Active Ingredient(s): | .005; 40 mg/mL; mg/mL & nbsp; prilocaine hydrochloride and epinephrine bitartrate |
| Administration Route(s): | DENTAL |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Citanest Forte
| Product NDC: | 66312-540 |
| Labeler Name: | Dentsply Pharmaceutical Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA021383 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19651118 |
Package Information of Citanest Forte
| Package NDC: | 66312-540-16 |
| Package Description: | 50 CARTRIDGE in 1 CARTON (66312-540-16) > 1.7 mL in 1 CARTRIDGE |
NDC Information of Citanest Forte
| NDC Code | 66312-540-16 |
| Proprietary Name | Citanest Forte |
| Package Description | 50 CARTRIDGE in 1 CARTON (66312-540-16) > 1.7 mL in 1 CARTRIDGE |
| Product NDC | 66312-540 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | prilocaine hydrochloride and epinephrine bitartrate |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | DENTAL |
| Start Marketing Date | 19651118 |
| Marketing Category Name | NDA |
| Labeler Name | Dentsply Pharmaceutical Inc. |
| Substance Name | EPINEPHRINE BITARTRATE; PRILOCAINE HYDROCHLORIDE |
| Strength Number | .005; 40 |
| Strength Unit | mg/mL; mg/mL |
| Pharmaceutical Classes | Amide Local Anesthetic [EPC],Amides [Chemical/Ingredient],Local Anesthesia [PE],Adrenergic alpha-Agonists [MoA],Adrenergic beta-Agonists [MoA],alpha-Adrenergic Agonist [EPC],beta-Adrenergic Agonist [EPC],Catecholamine [EPC],Catecholamines [Chemical/Ingredient] |
