NDC 86101-020 - Praziquantel
This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
- Product NDC
- 86101-020
- Package NDCs from labels
- 86101-020-21, 86101-020-50, 86101-020-13
- Manufacturer
- FELIX PHARMACEUTICALS PRIVATE LIMITED
- Effective date
- 2026-01-13
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Praziquantel - FELIX PHARMACEUTICALS PRIVATE LIMITED | FELIX PHARMACEUTICALS PRIVATE LIMITED | 2026-01-13 | Prescription Animal Drug Label |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 86101-020-13 | Praziquantel | 150 in 1 BOTTLE | TABLET, CHEWABLE | 150 | 1 | |
| 86101-020-21 | Praziquantel | 3 in 1 BOTTLE | TABLET, CHEWABLE | 3 | 1 | |
| 86101-020-50 | Praziquantel | 50 in 1 BOTTLE | TABLET, CHEWABLE | 50 | 1 |
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| PRAZIQUANTEL | PRAZIQUANTEL | Par Health USA, LLC | 16f2b9c4-a260-4a31-bd52-e5945913246c | 2026-08-12 | Warnings, Adverse reactions | 6490C9U457 |
| Biltricide | PRAZIQUANTEL | Bayer HealthCare Pharmaceuticals Inc. | 34ce1cdd-648e-4f1e-8512-bf3d4cc22eb9 | 2026-03-02 | Warnings, Adverse reactions | 6490C9U457 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.