Product NDC: | 21695-368 |
Proprietary Name: | PILOCARPINE HYDROCHLORIDE |
Non Proprietary Name: | PILOCARPINE HYDROCHLORIDE |
Active Ingredient(s): | 10 mg/mL & nbsp; PILOCARPINE HYDROCHLORIDE |
Administration Route(s): | CONJUNCTIVAL |
Dosage Form(s): | SOLUTION/ DROPS |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 21695-368 |
Labeler Name: | Rebel Distributors Corp |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA200890 |
Marketing Category: | NDA |
Start Marketing Date: | 20100622 |
Package NDC: | 21695-368-01 |
Package Description: | 1 BOTTLE, PLASTIC in 1 CARTON (21695-368-01) > 15 mL in 1 BOTTLE, PLASTIC |
NDC Code | 21695-368-01 |
Proprietary Name | PILOCARPINE HYDROCHLORIDE |
Package Description | 1 BOTTLE, PLASTIC in 1 CARTON (21695-368-01) > 15 mL in 1 BOTTLE, PLASTIC |
Product NDC | 21695-368 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | PILOCARPINE HYDROCHLORIDE |
Dosage Form Name | SOLUTION/ DROPS |
Route Name | CONJUNCTIVAL |
Start Marketing Date | 20100622 |
Marketing Category Name | NDA |
Labeler Name | Rebel Distributors Corp |
Substance Name | PILOCARPINE HYDROCHLORIDE |
Strength Number | 10 |
Strength Unit | mg/mL |
Pharmaceutical Classes | Cholinergic Agonists [MoA],Cholinergic Muscarinic Agonists [MoA],Cholinergic Receptor Agonist [EPC] |