Pentoxifylline
- Product NDC
- 68071-4532
- 11-digit product format
- 680714532
- Labeler code
- 68071
- Product ID
- 68071-4532_bbb815a8-1b46-3897-e053-2a95a90a6e39
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Pentoxifylline
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA075028
- Marketing category
- ANDA
- Marketing start
- 2014-08-22
- 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
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 68071-4532-9 | Pentoxifylline | 90 in 1 BOTTLE | TABLET, EXTENDED RELEASE | 90 | | 5 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68071-4532 | PENTOXIFYLLINE TABLET, EXTENDED RELEASE [NUCARE PHARMACEUTICALS,INC.] | 5 | Legacy NDC, 1 package rows | 20240612_73a6351c-5a8d-abbf-e053-2991aa0a5382.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68071-4532-9 | 68071453209 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (68071-4532-9) | 2018-08-17 | 0000-00-00 | No | No | Current |