Product NDC: | 61314-206 |
Proprietary Name: | PILOCARPINE HYDROCHLORIDE |
Non Proprietary Name: | pilocarpine hydrochloride |
Active Ingredient(s): | 40 mg/mL & nbsp; pilocarpine hydrochloride |
Administration Route(s): | OPHTHALMIC |
Dosage Form(s): | SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 61314-206 |
Labeler Name: | Falcon Pharmaceuticals, Ltd. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA200890 |
Marketing Category: | NDA |
Start Marketing Date: | 19960221 |
Package NDC: | 61314-206-15 |
Package Description: | 15 mL in 1 BOTTLE (61314-206-15) |
NDC Code | 61314-206-15 |
Proprietary Name | PILOCARPINE HYDROCHLORIDE |
Package Description | 15 mL in 1 BOTTLE (61314-206-15) |
Product NDC | 61314-206 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | pilocarpine hydrochloride |
Dosage Form Name | SOLUTION |
Route Name | OPHTHALMIC |
Start Marketing Date | 19960221 |
Marketing Category Name | NDA |
Labeler Name | Falcon Pharmaceuticals, Ltd. |
Substance Name | PILOCARPINE HYDROCHLORIDE |
Strength Number | 40 |
Strength Unit | mg/mL |
Pharmaceutical Classes | Cholinergic Agonists [MoA],Cholinergic Muscarinic Agonists [MoA],Cholinergic Receptor Agonist [EPC] |