Product NDC: | 17478-045 |
Proprietary Name: | Tetracaine |
Non Proprietary Name: | Tetracaine HCl |
Active Ingredient(s): | 10 mg/mL & nbsp; Tetracaine HCl |
Administration Route(s): | SUBARACHNOID |
Dosage Form(s): | INJECTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 17478-045 |
Labeler Name: | Akorn, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED DRUG OTHER |
Start Marketing Date: | 20100601 |
Package NDC: | 17478-045-32 |
Package Description: | 25 AMPULE in 1 CARTON (17478-045-32) > 2 mL in 1 AMPULE |
NDC Code | 17478-045-32 |
Proprietary Name | Tetracaine |
Package Description | 25 AMPULE in 1 CARTON (17478-045-32) > 2 mL in 1 AMPULE |
Product NDC | 17478-045 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Tetracaine HCl |
Dosage Form Name | INJECTION |
Route Name | SUBARACHNOID |
Start Marketing Date | 20100601 |
Marketing Category Name | UNAPPROVED DRUG OTHER |
Labeler Name | Akorn, Inc. |
Substance Name | TETRACAINE HYDROCHLORIDE |
Strength Number | 10 |
Strength Unit | mg/mL |
Pharmaceutical Classes | Ester Local Anesthetic [EPC],Esters [Chemical/Ingredient],Local Anesthesia [PE] |