| NDC Code | 71335-2094-1 |
|---|
| Package Description | 30 TABLET, FILM COATED in 1 BOTTLE (71335-2094-1) |
|---|
| Product NDC | 71335-2094 |
|---|
| 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 | 20190813 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA212377 |
|---|
| Manufacturer | Bryant Ranch Prepack |
|---|
| Substance Name | PILOCARPINE HYDROCHLORIDE |
|---|
| Strength | 5 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Cholinergic Agonists [MoA], Cholinergic Muscarinic Agonists [MoA], Cholinergic Receptor Agonist [EPC] |
|---|