Product NDC: | 0065-0215 |
Proprietary Name: | PILOPINE HS |
Non Proprietary Name: | pilocarpine hydrochloride |
Active Ingredient(s): | 40 mg/g & nbsp; pilocarpine hydrochloride |
Administration Route(s): | OPHTHALMIC |
Dosage Form(s): | GEL |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0065-0215 |
Labeler Name: | Alcon Laboratories, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA018796 |
Marketing Category: | NDA |
Start Marketing Date: | 19850115 |
Package NDC: | 0065-0215-35 |
Package Description: | 4 g in 1 TUBE (0065-0215-35) |
NDC Code | 0065-0215-35 |
Proprietary Name | PILOPINE HS |
Package Description | 4 g in 1 TUBE (0065-0215-35) |
Product NDC | 0065-0215 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | pilocarpine hydrochloride |
Dosage Form Name | GEL |
Route Name | OPHTHALMIC |
Start Marketing Date | 19850115 |
Marketing Category Name | NDA |
Labeler Name | Alcon Laboratories, Inc. |
Substance Name | PILOCARPINE HYDROCHLORIDE |
Strength Number | 40 |
Strength Unit | mg/g |
Pharmaceutical Classes | Cholinergic Agonists [MoA],Cholinergic Muscarinic Agonists [MoA],Cholinergic Receptor Agonist [EPC] |