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Tetracaine Hydrochloride
Tetracaine Hydrochloride - 0065-0741-12 - (tetracaine hydrochloride)
Drug Information of Tetracaine Hydrochloride
| Product NDC: | 0065-0741 |
| Proprietary Name: | Tetracaine Hydrochloride |
| Non Proprietary Name: | tetracaine hydrochloride |
| Active Ingredient(s): | 5 mg/mL & nbsp; tetracaine hydrochloride |
| Administration Route(s): | OPHTHALMIC |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Tetracaine Hydrochloride
| Product NDC: | 0065-0741 |
| Labeler Name: | Alcon Laboratories, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 19690328 |
Package Information of Tetracaine Hydrochloride
| Package NDC: | 0065-0741-12 |
| Package Description: | 12 BOTTLE, DROPPER in 1 CARTON (0065-0741-12) > 2 mL in 1 BOTTLE, DROPPER |
NDC Information of Tetracaine Hydrochloride
| NDC Code | 0065-0741-12 |
| Proprietary Name | Tetracaine Hydrochloride |
| Package Description | 12 BOTTLE, DROPPER in 1 CARTON (0065-0741-12) > 2 mL in 1 BOTTLE, DROPPER |
| Product NDC | 0065-0741 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | tetracaine hydrochloride |
| Dosage Form Name | SOLUTION |
| Route Name | OPHTHALMIC |
| Start Marketing Date | 19690328 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Alcon Laboratories, Inc. |
| Substance Name | TETRACAINE HYDROCHLORIDE |
| Strength Number | 5 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Ester Local Anesthetic [EPC],Esters [Chemical/Ingredient],Local Anesthesia [PE] |
