PENTOXIFYLLINE
- Product NDC
- 0615-8305
- 11-digit product format
- 006158305
- Labeler code
- 0615
- Product ID
- 0615-8305_834b9079-0207-47f4-b520-e0b8071c8f9a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- PENTOXIFYLLINE
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- NCS HealthCare of KY, LLC dba Vangard Labs
- Application
- ANDA075191
- Marketing category
- ANDA
- Marketing start
- 1999-06-10
- 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
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0615-8305-39 | 00615830539 | 30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (0615-8305-39) | 2019-07-02 | 0000-00-00 | No | No | Current |