PENTOXIFYLLINE
- Product NDC
- 68788-9742
- 11-digit product format
- 687889742
- Labeler code
- 68788
- Product ID
- 68788-9742_8109dc20-fb1b-4a0b-961a-3c77efe9f16f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- PENTOXIFYLLINE
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals, Inc.
- Application
- ANDA075191
- Marketing category
- ANDA
- Marketing start
- 2012-09-28
- Marketing end
- 0000-00-00
- Substance
- PENTOXIFYLLINE
- Active strength
- 400 mg/1
- Pharmacologic classes
- Blood Viscosity Reducer [EPC],Hematologic Activity Alteration [PE]
- NDC exclude flag
- E
- Listing certified through
- 2018-12-31
- Current FDA listing
- Historical FDA.report record