Pentoxifylline - Pentoxifylline
Navigation: NDC > Supplier starting with: U > UDL LABORATORIES, INC.| Field | Value |
|---|---|
| NDC Code: | 51079-889 |
| Proprietary Name: | Pentoxifylline |
| Suffix: | |
| Non-Proprietary Name: | Pentoxifylline |
| Dosage Form: | TABLET, FILM COATED, EXTENDED RELEASE |
| Method: | ORAL |
| Original Marketing Date: | 23-07-2010 |
| Category Name: | ANDA |
| Application Number: | ANDA074425 |
| Labeler: | UDL LABORATORIES, INC. |
| Substance Name: | PENTOXIFYLLINE |
| Active Numerator Strength: | 400 |
| Active Ingredient Unit: | mg/1 |
| Pharm Classes: | Blood Viscosity Reducer [EPC],Hematologic Activity Alteration [PE] |
| DEA Schedule: |