Product NDC: | 61314-016 |
Proprietary Name: | Proparacaine Hydrochloride |
Non Proprietary Name: | Proparacaine Hydrochloride |
Active Ingredient(s): | 5 mg/mL & nbsp; Proparacaine Hydrochloride |
Administration Route(s): | OPHTHALMIC |
Dosage Form(s): | SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 61314-016 |
Labeler Name: | Falcon Pharmaceuticals, Ltd. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA080027 |
Marketing Category: | ANDA |
Start Marketing Date: | 20000605 |
Package NDC: | 61314-016-01 |
Package Description: | 15 mL in 1 BOTTLE (61314-016-01) |
NDC Code | 61314-016-01 |
Proprietary Name | Proparacaine Hydrochloride |
Package Description | 15 mL in 1 BOTTLE (61314-016-01) |
Product NDC | 61314-016 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Proparacaine Hydrochloride |
Dosage Form Name | SOLUTION |
Route Name | OPHTHALMIC |
Start Marketing Date | 20000605 |
Marketing Category Name | ANDA |
Labeler Name | Falcon Pharmaceuticals, Ltd. |
Substance Name | PROPARACAINE HYDROCHLORIDE |
Strength Number | 5 |
Strength Unit | mg/mL |
Pharmaceutical Classes | Local Anesthesia [PE],Local Anesthetic [EPC] |