| NDC Code | 10135-680-01 |
|---|
| Package Description | 100 TABLET, FILM COATED in 1 BOTTLE (10135-680-01) |
|---|
| Product NDC | 10135-680 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Pilocarpine Hydrochloride |
|---|
| Non-Proprietary Name | Pilocarpine Hydrochloride |
|---|
| Dosage Form | TABLET, FILM COATED |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20190201 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA076963 |
|---|
| Manufacturer | Marlex Pharmaceuticals Inc |
|---|
| Substance Name | PILOCARPINE HYDROCHLORIDE |
|---|
| Strength | 5 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Cholinergic Agonists [MoA],Cholinergic Muscarinic Agonists [MoA],Cholinergic Receptor Agonist [EPC] |
|---|