HALOPERIDOL
- Product NDC
- 35573-442
- 11-digit product format
- 355730442
- Labeler code
- 35573
- Product ID
- 35573-442_dcd9c7a9-13ee-4740-890a-1d01473b30f2
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- HALOPERIDOL
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Burel Pharmaceuticals, LLC
- Application
- ANDA071132
- Marketing category
- ANDA
- Marketing start
- 2021-05-31
- Marketing end
- 0000-00-00
- Substance
- HALOPERIDOL
- Active strength
- 10 mg/1
- Pharmacologic classes
- Typical Antipsychotic [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 35573-442 | HALOPERIDOL TABLET [BUREL PHARMACEUTICALS, LLC] | 6 | Legacy NDC | 20210606_43bb14ed-d0c3-43be-92c4-ccb913737390.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 35573-442-02 | 35573044202 | 100 TABLET in 1 BOTTLE (35573-442-02) | 100 tablet | 2021-05-31 | 0000-00-00 | No | No | Current |