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Pentoxifylline
Pentoxifylline - 51079-889-20 - (Pentoxifylline)
Drug Information of Pentoxifylline
| Product NDC: | 51079-889 |
| Proprietary Name: | Pentoxifylline |
| Non Proprietary Name: | Pentoxifylline |
| Active Ingredient(s): | 400 mg/1 & nbsp; Pentoxifylline |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED, EXTENDED RELEASE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Pentoxifylline
| Product NDC: | 51079-889 |
| Labeler Name: | UDL Laboratories, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA074425 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20100723 |
Package Information of Pentoxifylline
| Package NDC: | 51079-889-20 |
| Package Description: | 100 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-889-20) > 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (51079-889-01) |
NDC Information of Pentoxifylline
| NDC Code | 51079-889-20 |
| Proprietary Name | Pentoxifylline |
| Package Description | 100 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-889-20) > 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (51079-889-01) |
| Product NDC | 51079-889 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Pentoxifylline |
| Dosage Form Name | TABLET, FILM COATED, EXTENDED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20100723 |
| Marketing Category Name | ANDA |
| Labeler Name | UDL Laboratories, Inc. |
| Substance Name | PENTOXIFYLLINE |
| Strength Number | 400 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Blood Viscosity Reducer [EPC],Hematologic Activity Alteration [PE] |
