Haloperidol
- Product NDC
- 50090-6017
- 11-digit product format
- 500906017
- Labeler code
- 50090
- Product ID
- 50090-6017_263042c4-fd7a-43b8-b01d-bba99dd39338
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Haloperidol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA211061
- Marketing category
- ANDA
- Marketing start
- 2020-01-09
- Marketing end
- 0000-00-00
- Substance
- HALOPERIDOL
- Active strength
- 5 mg/1
- Pharmacologic classes
- Typical Antipsychotic [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 50090-6017-0 | Haloperidol | 33 in 1 CARTON | TABLET | 33 | | 2 |
| 50090-6017-0 | Haloperidol | 1 in 1 BLISTER PACK | TABLET | 1 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-6017 | HALOPERIDOL TABLET [A-S MEDICATION SOLUTIONS] | 2 | Legacy NDC, 2 package rows | 20220630_4c7cea51-f0fa-4fa1-8f7f-9f04f246d077.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-6017-0 | 50090601700 | 33 BLISTER PACK in 1 CARTON (50090-6017-0) > 1 TABLET in 1 BLISTER PACK | 33 blister pack | 2022-06-24 | 0000-00-00 | No | No | Current |