PENTOXIFYLLINE
- Product NDC
- 70518-1285
- 11-digit product format
- 705181285
- Labeler code
- 70518
- Product ID
- 70518-1285_e3b37ec9-aece-e4c8-e053-2a95a90a2f2f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- PENTOXIFYLLINE
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA075191
- Marketing category
- ANDA
- Marketing start
- 2018-07-06
- 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 |
|---|
| 70518-1285-0 | 70518128500 | 180 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-1285-0) | 2018-07-06 | 0000-00-00 | No | No | Current |