| NDC Code | 53808-0758-1 |
|---|
| Package Description | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (53808-0758-1) |
|---|
| Product NDC | 53808-0758 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Pentoxifylline |
|---|
| Non-Proprietary Name | Pentoxifylline |
|---|
| Dosage Form | TABLET, FILM COATED, EXTENDED RELEASE |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20090701 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA074425 |
|---|
| Manufacturer | State of Florida DOH Central Pharmacy |
|---|
| Substance Name | PENTOXIFYLLINE |
|---|
| Strength | 400 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Blood Viscosity Reducer [EPC],Hematologic Activity Alteration [PE] |
|---|