Pentoxifylline 00904-5448
Product NDC
00904-5448- Manufacturer
- Major Pharmaceuticals
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- June 10, 1999
- Listing Expires
- December 31, 2026
- Application
- ANDA075191
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Pentoxifylline | 400 mg/1 |
Drug Class
Blood Viscosity Reducer [EPC]Blood Viscosity Reducer [EPC]Hematologic Activity Alteration [PE]
Packaging Options(1)
100 BLISTER PACK in 1 CARTON (0904-5448-61) / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK