| 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: | 54799-504-05 |
| Package Description: | 5 mL in 1 BOTTLE, DROPPER (54799-504-05) |
| NDC Code | 54799-504-05 |
| Proprietary Name | TetraVisc Forte |
| Package Description | 5 mL in 1 BOTTLE, DROPPER (54799-504-05) |
| 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] |