Haloperidol
- Product NDC
- 50436-0233
- 11-digit product format
- 504360233
- Labeler code
- 50436
- Product ID
- 50436-0233_fa7eb5bf-7a20-4183-ba41-e8d5c6c4b3a8
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Haloperidol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Unit Dose Services
- Application
- ANDA077580
- Marketing category
- ANDA
- Marketing start
- 2008-01-03
- Marketing end
- 0000-00-00
- Substance
- HALOPERIDOL
- Active strength
- 5 mg/1
- Pharmacologic classes
- Typical Antipsychotic [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- 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 |
|---|
| 50436-0233-4 | Haloperidol | 14 in 1 BOTTLE | TABLET | 14 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50436-0233 | HALOPERIDOL TABLET [UNIT DOSE SERVICES] | 3 | Legacy NDC, 1 package rows | 20181010_6ca34b20-df63-46a0-9d31-fe2bd3311a18.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 50436-0233-4 | 50436023304 | 14 in 1 BOTTLE | Historical |