HALOPERIDOL
- Product NDC
- 35573-440
- 11-digit product format
- 355730440
- Labeler code
- 35573
- Product ID
- 35573-440_553e9517-6ce2-4105-99fc-02de9c95ad6f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- HALOPERIDOL
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Burel Pharmaceuticals, LLC
- Application
- ANDA071130
- Marketing category
- ANDA
- Marketing start
- 2021-05-31
- Marketing end
- 0000-00-00
- Substance
- HALOPERIDOL
- Active strength
- 2 mg/1
- Pharmacologic classes
- Typical Antipsychotic [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 35573-440-02 | 35573044002 | 100 TABLET in 1 BOTTLE (35573-440-02) | 100 tablet | 2021-05-31 | 0000-00-00 | No | No | Current |