PENTOXIFYLLINE
- Product NDC
- 60429-703
- 11-digit product format
- 604290703
- Labeler code
- 60429
- Product ID
- 60429-703_933cc7a5-34ed-20b2-e053-2a95a90ae492
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- PENTOXIFYLLINE
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Golden State Medical Supply, Inc.
- Application
- ANDA075191
- Marketing category
- ANDA
- Marketing start
- 1999-06-09
- 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
- 2020-12-31
- 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 |
|---|
| 60429-703-05 | 60429070305 | 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (60429-703-05) | 2001-06-18 | 0000-00-00 | No | No | Current |