PENTOXIFYLLINE
- Product NDC
- 66267-710
- 11-digit product format
- 662670710
- Labeler code
- 66267
- Product ID
- 66267-710_9cbda98b-76b5-4fc3-e053-2995a90a42b1
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- PENTOXIFYLLINE
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals, Inc.
- 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
- 2021-12-31
- 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 |
|---|
| 66267-710-30 | 66267071030 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (66267-710-30) | 2016-12-29 | 0000-00-00 | No | No | Current |
| 66267-710-60 | 66267071060 | 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (66267-710-60) | 2016-12-29 | 0000-00-00 | No | No | Current |
| 66267-710-90 | 66267071090 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (66267-710-90) | 2016-12-29 | 0000-00-00 | No | No | Current |