| NDC Code | 16571-689-01 |
|---|
| Package Description | 100 TABLET, FILM COATED in 1 BOTTLE (16571-689-01) |
|---|
| Product NDC | 16571-689 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Carbidopa, Levodopa And Entacapone |
|---|
| Non-Proprietary Name | Carbidopa, Levodopa And Entacapone |
|---|
| Dosage Form | TABLET, FILM COATED |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20210805 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA213212 |
|---|
| Manufacturer | Rising Pharma Holdings, Inc. |
|---|
| Substance Name | CARBIDOPA; ENTACAPONE; LEVODOPA |
|---|
| Strength | 12.5; 200; 50 |
|---|
| Strength Unit | mg/1; mg/1; mg/1 |
|---|
| Pharmacy Classes | Amino Acids, Aromatic [CS], Aromatic Amino Acid [EPC], Catechol O-Methyltransferase Inhibitors [MoA], Catechol-O-Methyltransferase Inhibitor [EPC] |
|---|