Haloperidol
- Product NDC
- 17856-0730
- 11-digit product format
- 178560730
- Labeler code
- 17856
- Product ID
- 17856-0730_186876c9-d435-44b4-ad71-acf5f1a1167a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Haloperidol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- ATLANTIC BIOLOGICALS CORP.
- Application
- ANDA071173
- Marketing category
- ANDA
- Marketing start
- 2019-11-25
- Marketing end
- 0000-00-00
- Substance
- HALOPERIDOL
- Active strength
- 5 mg/1
- Pharmacologic classes
- Typical Antipsychotic [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- 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 |
|---|
| 17856-0730-1 | Haloperidol | 100 in 1 BOX, UNIT-DOSE | TABLET | 100 | | 1 |
| 17856-0730-1 | Haloperidol | 1 in 1 POUCH | TABLET | 1 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 17856-0730 | HALOPERIDOL TABLET [ATLANTIC BIOLOGICALS CORP.] | 1 | Legacy NDC, 2 package rows | 20210317_76d56670-6e54-4321-bf4a-0d75692fefd1.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 |
|---|
| 17856-0730-1 | 17856073001 | 100 POUCH in 1 BOX, UNIT-DOSE (17856-0730-1) > 1 TABLET in 1 POUCH | 100 pouch | 2021-03-15 | 0000-00-00 | No | No | Current |