NDC 71052-651-10 - Romifidine HCl
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
- 71052-651
- Requested NDC
- 71052-651-10
- Package NDCs from labels
- 71052-651-01, 71052-651-50, 71052-651-25, 71052-651-05, 71052-651-10
- Manufacturer
- DARMERICA, LLC
- Effective date
- 2026-10-07
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Romifidine HCl - DARMERICA, LLC | DARMERICA, LLC | 2026-10-07 | BULK INGREDIENT - ANIMAL DRUG |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 71052-651-01 | Romifidine HCl | 0.1 kg in 1 PACKAGE | POWDER | 0.1 | 3 | |
| 71052-651-05 | Romifidine HCl | 0.005 kg in 1 PACKAGE | POWDER | 0.005 | 3 | |
| 71052-651-10 | Romifidine HCl | 0.01 kg in 1 PACKAGE | POWDER | 0.01 | 3 | |
| 71052-651-25 | Romifidine HCl | 0.025 kg in 1 PACKAGE | POWDER | 0.025 | 3 | |
| 71052-651-50 | Romifidine HCl | 0.05 kg in 1 PACKAGE | POWDER | 0.05 | 3 |
DailyMed Dashboard NDC Coverage#
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.