Haloperidol
- Product NDC
- 64725-0080
- 11-digit product format
- 647250080
- Labeler code
- 64725
- Product ID
- 64725-0080_2e6f2b3e-1cc5-4121-8354-a169da971973
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Haloperidol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- TYA Pharmaceuticals
- Application
- ANDA077580
- Marketing category
- ANDA
- Marketing start
- 2008-01-03
- Marketing end
- 0000-00-00
- Substance
- HALOPERIDOL
- Active strength
- 10 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 |
|---|---|---|---|---|---|
| 64725-0080-1 | 2019-11-27 | C162847 | 48780-1 | 9855e2a2-3abc-60a7-e053-dbdaa90a05bd | Haloperidol Tablets, USP |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 64725-0080-1 | Haloperidol | 100 in 1 BOTTLE | TABLET | 100 | 2 |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|---|---|---|---|---|
| HALOPERIDOL | ACTIVE INGREDIENT | J6292F8L3D | HALOPERIDOL TABLET [TYA PHARMACEUTICALS] | 2 | |
| HALOPERIDOL | ACTIVE MOIETY | J6292F8L3D | HALOPERIDOL TABLET [TYA PHARMACEUTICALS] | 2 | |
| CALCIUM PHOSPHATE, DIBASIC, DIHYDRATE | INACTIVE INGREDIENT | O7TSZ97GEP | HALOPERIDOL TABLET [TYA PHARMACEUTICALS] | 2 | |
| CALCIUM STEARATE | INACTIVE INGREDIENT | 776XM7047L | HALOPERIDOL TABLET [TYA PHARMACEUTICALS] | 2 | |
| D&C YELLOW NO. 10 | INACTIVE INGREDIENT | 35SW5USQ3G | HALOPERIDOL TABLET [TYA PHARMACEUTICALS] | 2 | |
| FD&C BLUE NO. 1 | INACTIVE INGREDIENT | H3R47K3TBD | HALOPERIDOL TABLET [TYA PHARMACEUTICALS] | 2 | |
| POVIDONE K30 | INACTIVE INGREDIENT | U725QWY32X | HALOPERIDOL TABLET [TYA PHARMACEUTICALS] | 2 | |
| SODIUM STARCH GLYCOLATE TYPE A POTATO | INACTIVE INGREDIENT | 5856J3G2A2 | HALOPERIDOL TABLET [TYA PHARMACEUTICALS] | 2 | |
| STARCH, CORN | INACTIVE INGREDIENT | O8232NY3SJ | HALOPERIDOL TABLET [TYA PHARMACEUTICALS] | 2 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 64725-0080 | HALOPERIDOL TABLET [TYA PHARMACEUTICALS] | 2 | Legacy NDC, 1 package rows | 20140928_def76be8-49c2-4e7d-832f-2bfb1fc090ac.zip |
DailyMed RxNorm Mappings#
| RxCUI | RxNorm string | TTY | DailyMed | SPL version |
|---|---|---|---|---|
| 314035 | haloperidol 10 MG Oral Tablet | PSN | def76be8-49c2-4e7d-832f-2bfb1fc090ac | 2 |
| 314035 | haloperidol 10 MG Oral Tablet | SCD | def76be8-49c2-4e7d-832f-2bfb1fc090ac | 2 |
Packages#
| Package NDC | 11-digit format | Description | Status |
|---|---|---|---|
| 64725-0080-1 | 64725008001 | 100 in 1 BOTTLE | Historical |