Haldol is a Intramuscular Injection in the Human Prescription Drug category. It is labeled and distributed by Janssen Pharmaceuticals, Inc.. The primary component is Haloperidol Lactate.
Product ID | 50458-255_3ba71ec4-639a-11ea-b9d7-9d1ffc2ca371 |
NDC | 50458-255 |
Product Type | Human Prescription Drug |
Proprietary Name | Haldol |
Generic Name | Haloperidol |
Dosage Form | Injection |
Route of Administration | INTRAMUSCULAR |
Marketing Start Date | 1971-05-18 |
Marketing Category | NDA / NDA |
Application Number | NDA015923 |
Labeler Name | Janssen Pharmaceuticals, Inc. |
Substance Name | HALOPERIDOL LACTATE |
Active Ingredient Strength | 5 mg/mL |
Pharm Classes | Typical Antipsychotic [EPC] |
NDC Exclude Flag | N |
Listing Certified Through | 2021-12-31 |
Marketing Start Date | 1971-05-18 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | NDA |
Application Number | NDA015923 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | ML |
Marketing Start Date | 1971-05-18 |
Ingredient | Strength |
---|---|
HALOPERIDOL LACTATE | 5 mg/mL |
SPL SET ID: | 27cfe684-7d11-4f37-9c8b-b2bdd6b5348e |
Manufacturer | |
UNII | |
RxNorm Concept Unique ID - RxCUI |
NDC | Brand Name | Generic Name |
---|---|---|
50458-255 | Haldol | Haldol |
0121-0581 | Haloperidol | Haloperidol |
0378-0214 | Haloperidol | haloperidol |
0378-0257 | Haloperidol | haloperidol |
0378-0327 | Haloperidol | haloperidol |
0378-0334 | Haloperidol | haloperidol |
0378-0335 | Haloperidol | haloperidol |
0378-0351 | Haloperidol | haloperidol |
0615-2594 | Haloperidol | Haloperidol |
0615-2595 | Haloperidol | Haloperidol |
0615-2596 | Haloperidol | Haloperidol |
0615-2597 | Haloperidol | Haloperidol |
0404-9871 | Haloperidol Lactate | Haloperidol |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
HALDOL 72192450 0777269 Live/Registered |
McNeil Laboratories, Incorporated 1964-05-01 |