Product NDC: | 61314-355 |
Proprietary Name: | Tropicamide |
Non Proprietary Name: | Tropicamide |
Active Ingredient(s): | 10 mg/mL & nbsp; Tropicamide |
Administration Route(s): | OPHTHALMIC |
Dosage Form(s): | SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 61314-355 |
Labeler Name: | Sandoz Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA084306 |
Marketing Category: | ANDA |
Start Marketing Date: | 20000613 |
Package NDC: | 61314-355-01 |
Package Description: | 3 mL in 1 BOTTLE, PLASTIC (61314-355-01) |
NDC Code | 61314-355-01 |
Proprietary Name | Tropicamide |
Package Description | 3 mL in 1 BOTTLE, PLASTIC (61314-355-01) |
Product NDC | 61314-355 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Tropicamide |
Dosage Form Name | SOLUTION |
Route Name | OPHTHALMIC |
Start Marketing Date | 20000613 |
Marketing Category Name | ANDA |
Labeler Name | Sandoz Inc. |
Substance Name | TROPICAMIDE |
Strength Number | 10 |
Strength Unit | mg/mL |
Pharmaceutical Classes | Anticholinergic [EPC],Cholinergic Antagonists [MoA] |