NDC 16571-856 – Pentoxifylline
Pentoxifylline 400 mg/1 · Tablet, Extended Release · Oral
Product NDC16571-856
Product details
- Brand name
- Pentoxifylline
- Generic name
- Pentoxifylline
- Labeler
- Rising Pharma Holdings, Inc.
- Dosage form
- Tablet, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA074425
- Marketed since
- June 11, 2024
- Listing expires
- December 31, 2027
- Pharmacologic class
- Blood Viscosity Reducer
Active ingredients
- Pentoxifylline 400 mg/1
Uses, dosage, side effects and warnings for Pentoxifylline →
Package NDC codes (5)
| Package NDC | Description | Since |
|---|---|---|
| 16571-856-01 | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (16571-856-01) | Jun 5, 2026 |
| 16571-856-05 | 50 BLISTER PACK in 1 CARTON (16571-856-05) / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK | Jun 5, 2026 |
| 16571-856-11 | 10 BLISTER PACK in 1 CARTON (16571-856-11) / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK | Jun 5, 2026 |
| 16571-856-50 | 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (16571-856-50) | Jun 5, 2026 |
| 16571-856-90 | 1 BLISTER PACK in 1 CARTON (16571-856-90) / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK | Jun 5, 2026 |
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