Haloperidol
- Product NDC
- 50090-3468
- 11-digit product format
- 500903468
- Labeler code
- 50090
- Product ID
- 50090-3468_ba45a944-656b-4691-a6ca-4dee73cba370
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- haloperidol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA070278
- Marketing category
- ANDA
- Marketing start
- 1986-06-10
- Marketing end
- 0000-00-00
- Substance
- HALOPERIDOL
- Active strength
- 5 mg/1
- Pharmacologic classes
- Typical Antipsychotic [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- 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 |
|---|
| 50090-3468-0 | Haloperidol | 33 in 1 CARTON | TABLET | 33 | | 1 |
| 50090-3468-0 | Haloperidol | 1 in 1 BLISTER PACK | TABLET | 1 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-3468 | HALOPERIDOL TABLET [A-S MEDICATION SOLUTIONS] | 1 | Legacy NDC, 2 package rows | 20181010_6b9b2f65-b953-46e2-a5ef-20f1854857e7.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 50090-3468-0 | 50090346800 | 33 in 1 CARTON | Historical |