Application 071237
- Type
- ANDA
- Sponsor
- VINTAGE
Application Products#
| Product | Drug | Ingredient | Form | Strength | Reference drug | Reference standard |
|---|---|---|---|---|---|---|
| 001 | HALOPERIDOL | HALOPERIDOL | TABLET;ORAL | 10MG | No | No |
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 |
|---|---|---|---|---|---|---|
| Haloperidol | HALOPERIDOL LACTATE | Fresenius Kabi USA, LLC | b1ad2abd-a9d6-44e3-957b-36a73260f4f5 | 2022-01-25 | Boxed warning, Warnings, Adverse reactions | Haloperidol |
| HALOPERIDOL | HALOPERIDOL LACTATE | HF Acquisition Co LLC, DBA HealthFirst | beb6d1cf-98db-d0a5-e053-2995a90ace90 | 2021-03-29 | Boxed warning, Warnings, Adverse reactions | HALOPERIDOL |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.