Product NDC: | 52125-502 |
Proprietary Name: | PILOCARPINE HYDROCHLORIDE |
Non Proprietary Name: | pilocarpine hydrochloride |
Active Ingredient(s): | 40 mg/1 & nbsp; pilocarpine hydrochloride |
Administration Route(s): | OPHTHALMIC |
Dosage Form(s): | SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 52125-502 |
Labeler Name: | REMEDYREPACK INC. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA200890 |
Marketing Category: | NDA |
Start Marketing Date: | 20130415 |
Package NDC: | 52125-502-01 |
Package Description: | 1 SOLUTION in 1 CARTON (52125-502-01) |
NDC Code | 52125-502-01 |
Proprietary Name | PILOCARPINE HYDROCHLORIDE |
Package Description | 1 SOLUTION in 1 CARTON (52125-502-01) |
Product NDC | 52125-502 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | pilocarpine hydrochloride |
Dosage Form Name | SOLUTION |
Route Name | OPHTHALMIC |
Start Marketing Date | 20130415 |
Marketing Category Name | NDA |
Labeler Name | REMEDYREPACK INC. |
Substance Name | PILOCARPINE HYDROCHLORIDE |
Strength Number | 40 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Cholinergic Agonists [MoA],Cholinergic Muscarinic Agonists [MoA],Cholinergic Receptor Agonist [EPC] |