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PENTOXIFYLLINE
PENTOXIFYLLINE - 68788-9742-3 - (PENTOXIFYLLINE)
Drug Information of PENTOXIFYLLINE
| Product NDC: | 68788-9742 |
| Proprietary Name: | PENTOXIFYLLINE |
| Non Proprietary Name: | PENTOXIFYLLINE |
| Active Ingredient(s): | 400 mg/1 & nbsp; PENTOXIFYLLINE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, EXTENDED RELEASE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of PENTOXIFYLLINE
| Product NDC: | 68788-9742 |
| Labeler Name: | Preferred Pharmaceuticals, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA075191 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20120928 |
Package Information of PENTOXIFYLLINE
| Package NDC: | 68788-9742-3 |
| Package Description: | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-9742-3) |
NDC Information of PENTOXIFYLLINE
| NDC Code | 68788-9742-3 |
| Proprietary Name | PENTOXIFYLLINE |
| Package Description | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-9742-3) |
| Product NDC | 68788-9742 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | PENTOXIFYLLINE |
| Dosage Form Name | TABLET, EXTENDED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20120928 |
| Marketing Category Name | ANDA |
| Labeler Name | Preferred Pharmaceuticals, Inc. |
| Substance Name | PENTOXIFYLLINE |
| Strength Number | 400 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Blood Viscosity Reducer [EPC],Hematologic Activity Alteration [PE] |
