Haloperidol
- Product NDC
- 65841-838
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Haloperidol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Zydus Lifesciences Limited
- Application
- ANDA077580
- Marketing category
- ANDA
- Substance
- HALOPERIDOL
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 65841-838-01 | 100 TABLET in 1 BOTTLE (65841-838-01) | 2023-02-01 | | No | Historical |
| 65841-838-10 | 1000 TABLET in 1 BOTTLE (65841-838-10) | 2023-02-01 | | No | Historical |
| 65841-838-77 | 10 BLISTER PACK in 1 CARTON (65841-838-77) / 10 TABLET in 1 BLISTER PACK (65841-838-30) | 2023-02-01 | | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Haloperidol Tablets, USP | Zydus Lifesciences Limited | 2024-11-30 | HUMAN PRESCRIPTION DRUG LABEL | 8 |