| NDC Code | 0115-5911-03 |
|---|
| Package Description | 1000 TABLET, FILM COATED in 1 BOTTLE (0115-5911-03) |
|---|
| Product NDC | 0115-5911 |
|---|
| 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 | 20070501 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA077248 |
|---|
| Manufacturer | Amneal Pharmaceuticals of New York LLC |
|---|
| Substance Name | PILOCARPINE HYDROCHLORIDE |
|---|
| Strength | 7.5 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Cholinergic Agonists [MoA], Cholinergic Muscarinic Agonists [MoA], Cholinergic Receptor Agonist [EPC] |
|---|