Product NDC: | 68788-0920 |
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) |
Product NDC: | 68788-0920 |
Labeler Name: | Preferred Pharmaceuticals, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED DRUG OTHER |
Start Marketing Date: | 20130516 |
Package NDC: | 68788-0920-1 |
Package Description: | 1 BOTTLE, DROPPER in 1 CARTON (68788-0920-1) > 15 mL in 1 BOTTLE, DROPPER |
NDC Code | 68788-0920-1 |
Proprietary Name | Tetracaine Hydrochloride |
Package Description | 1 BOTTLE, DROPPER in 1 CARTON (68788-0920-1) > 15 mL in 1 BOTTLE, DROPPER |
Product NDC | 68788-0920 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Tetracaine Hydrochloride |
Dosage Form Name | SOLUTION |
Route Name | OPHTHALMIC |
Start Marketing Date | 20130516 |
Marketing Category Name | UNAPPROVED DRUG OTHER |
Labeler Name | Preferred Pharmaceuticals, Inc. |
Substance Name | TETRACAINE HYDROCHLORIDE |
Strength Number | 5 |
Strength Unit | mg/mL |
Pharmaceutical Classes | Ester Local Anesthetic [EPC],Esters [Chemical/Ingredient],Local Anesthesia [PE] |