Haloperidol
- Product NDC
- 64725-0214
- 11-digit product format
- 647250214
- Labeler code
- 64725
- Product ID
- 64725-0214_f3a5ed5a-a76e-4b7a-91a8-5d5e0c3d33b8
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- haloperidol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- TYA Pharmaceuticals
- Application
- ANDA070278
- Marketing category
- ANDA
- Marketing start
- 1986-06-10
- Marketing end
- 0000-00-00
- Substance
- HALOPERIDOL
- Active strength
- 2 mg/1
- Pharmacologic classes
- Typical Antipsychotic [EPC]
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| d599bae4-cb25-0798-7468-31aa188fb750 | Product name | 7 | 20260304 |
| 6aae29ef-bf3c-3ebb-3bf1-10ee5424a22e | Product name | 2 | 20250114 |
| af58e43a-5792-c2c1-8e57-a2454df1f2c0 | Product name | 3 | 20240202 |
| ce329990-eb12-45a5-87d5-ce5ef054ca71 | Product name | 2 | 20190930 |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 64725-0214-1 | 2020-01-31 | C162847 | 48780-1 | 9d75b9d0-6529-f424-e053-dadaa90a57ce | 4771cba5-2b48-41dc-9c2b-199c55999d3a |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 64725-0214-1 | Haloperidol | 100 in 1 BOTTLE | TABLET | 100 | 4 |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|---|---|---|---|---|
| HALOPERIDOL | ACTIVE INGREDIENT | J6292F8L3D | HALOPERIDOL TABLET [TYA PHARMACEUTICALS] | 4 | |
| HALOPERIDOL | ACTIVE MOIETY | J6292F8L3D | HALOPERIDOL TABLET [TYA PHARMACEUTICALS] | 4 | |
| CELLULOSE, MICROCRYSTALLINE | INACTIVE INGREDIENT | OP1R32D61U | HALOPERIDOL TABLET [TYA PHARMACEUTICALS] | 4 | |
| FD&C YELLOW NO. 6 | INACTIVE INGREDIENT | H77VEI93A8 | HALOPERIDOL TABLET [TYA PHARMACEUTICALS] | 4 | |
| MAGNESIUM STEARATE | INACTIVE INGREDIENT | 70097M6I30 | HALOPERIDOL TABLET [TYA PHARMACEUTICALS] | 4 | |
| SILICON DIOXIDE | INACTIVE INGREDIENT | ETJ7Z6XBU4 | HALOPERIDOL TABLET [TYA PHARMACEUTICALS] | 4 | |
| SODIUM LAURYL SULFATE | INACTIVE INGREDIENT | 368GB5141J | HALOPERIDOL TABLET [TYA PHARMACEUTICALS] | 4 | |
| STARCH, CORN | INACTIVE INGREDIENT | O8232NY3SJ | HALOPERIDOL TABLET [TYA PHARMACEUTICALS] | 4 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 64725-0214 | HALOPERIDOL TABLET [TYA PHARMACEUTICALS] | 4 | Legacy NDC, 1 package rows | 20141110_4771cba5-2b48-41dc-9c2b-199c55999d3a.zip |
DailyMed RxNorm Mappings#
| RxCUI | RxNorm string | TTY | DailyMed | SPL version |
|---|---|---|---|---|
| 314034 | haloperidol 2 MG Oral Tablet | PSN | 4771cba5-2b48-41dc-9c2b-199c55999d3a | 4 |
| 310672 | haloperidol 5 MG Oral Tablet | PSN | 4771cba5-2b48-41dc-9c2b-199c55999d3a | 4 |
| 314034 | haloperidol 2 MG Oral Tablet | SCD | 4771cba5-2b48-41dc-9c2b-199c55999d3a | 4 |
| 310672 | haloperidol 5 MG Oral Tablet | SCD | 4771cba5-2b48-41dc-9c2b-199c55999d3a | 4 |
Packages#
| Package NDC | 11-digit format | Description | Status |
|---|---|---|---|
| 64725-0214-1 | 64725021401 | 100 in 1 BOTTLE | Historical |