Haloperidol
- Product NDC
- 17856-0581
- 11-digit product format
- 178560581
- Labeler code
- 17856
- Product ID
- 17856-0581_4e108b29-cccc-4c0f-baa3-9943c65fc801
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Haloperidol
- Dosage form
- SOLUTION, CONCENTRATE
- Route
- ORAL
- Labeler
- Atlantic Biologicals Corps
- Application
- ANDA073037
- Marketing category
- ANDA
- Marketing start
- 2009-11-10
- Marketing end
- 0000-00-00
- Substance
- HALOPERIDOL
- Active strength
- 2 mg/mL
- Pharmacologic classes
- Typical Antipsychotic [EPC]
- NDC exclude flag
- E
- Listing certified through
- 2018-12-31
- 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 |
|---|
| 17856-0581-5 | Haloperidol | 2.5 mL in 1 SYRINGE, PLASTIC | SOLUTION, CONCENTRATE | 2.5 | | 2 |
| 17856-0581-5 | Haloperidol | 48 in 1 CASE | SOLUTION, CONCENTRATE | 48 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 17856-0581 | HALOPERIDOL SOLUTION, CONCENTRATE [ATLANTIC BIOLOGICALS CORPS] | 2 | Legacy NDC, 2 package rows | 20170629_599a6800-b2a8-41da-8733-577b819291c7.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 17856-0581-5 | 17856058105 | 2.5 mL in 1 SYRINGE, PLASTIC | 2.5 ml | Historical |