Haloperidol
- Product NDC
- 70518-1269
- 11-digit product format
- 705181269
- Labeler code
- 70518
- Product ID
- 70518-1269_48c3d134-d4dd-a5fc-e063-6294a90acd5a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Haloperidol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA077580
- Marketing category
- ANDA
- Marketing start
- 2018-06-19
- Substance
- HALOPERIDOL
- Active strength
- 5 mg/1
- Pharmacologic classes
- Typical Antipsychotic [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Haloperidol
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| HALOPERIDOL | 5 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | J6292F8L3D |
| Rxcui | 310672 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 70518-1269-0 | Haloperidol | 30 in 1 BLISTER PACK | TABLET | 30 | | 16 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70518-1269 | HALOPERIDOL TABLET [REMEDYREPACK INC.] | 14 | Current NDC, Legacy NDC, 1 package rows | 20250510_58fa9328-b1c7-407c-b215-9887db90cb94.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 |
|---|
| 70518-1269-0 | 70518126900 | 30 TABLET in 1 BLISTER PACK (70518-1269-0) | 30 tablet | 2018-06-19 | 0000-00-00 | No | No | Current |