Pentoxifylline
- Product NDC
- 0615-4523
- 11-digit product format
- 006154523
- Labeler code
- 0615
- Product ID
- 0615-4523_e71a3614-e3ae-4979-b6d9-1556c2ca2161
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Pentoxifylline
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- NCS HealthCare of KY, Inc dba Vangard Labs
- Application
- ANDA074425
- Marketing category
- ANDA
- Marketing start
- 2009-09-21
- 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
- 2017-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#