Product NDC: | 54799-504 |
Proprietary Name: | TetraVisc Forte |
Non Proprietary Name: | Tetracaine Hydrochloride |
Active Ingredient(s): | 25 mg/5mL & nbsp; Tetracaine Hydrochloride |
Administration Route(s): | OPHTHALMIC |
Dosage Form(s): | LIQUID |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 54799-504 |
Labeler Name: | OCuSOFT, INC. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED DRUG OTHER |
Start Marketing Date: | 20090825 |
Package NDC: | 54799-504-01 |
Package Description: | .6 mL in 1 BOTTLE, DROPPER (54799-504-01) |
NDC Code | 54799-504-01 |
Proprietary Name | TetraVisc Forte |
Package Description | .6 mL in 1 BOTTLE, DROPPER (54799-504-01) |
Product NDC | 54799-504 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Tetracaine Hydrochloride |
Dosage Form Name | LIQUID |
Route Name | OPHTHALMIC |
Start Marketing Date | 20090825 |
Marketing Category Name | UNAPPROVED DRUG OTHER |
Labeler Name | OCuSOFT, INC. |
Substance Name | TETRACAINE HYDROCHLORIDE |
Strength Number | 25 |
Strength Unit | mg/5mL |
Pharmaceutical Classes | Ester Local Anesthetic [EPC],Esters [Chemical/Ingredient],Local Anesthesia [PE] |