Product NDC: | 50458-253 |
Proprietary Name: | Haldol Decanoate |
Non Proprietary Name: | Haloperidol Decanoate |
Active Ingredient(s): | 50 mg/mL & nbsp; Haloperidol Decanoate |
Administration Route(s): | INTRAMUSCULAR |
Dosage Form(s): | INJECTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 50458-253 |
Labeler Name: | Janssen Pharmaceuticals, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA018701 |
Marketing Category: | NDA |
Start Marketing Date: | 19860114 |
Package NDC: | 50458-253-01 |
Package Description: | 10 AMPULE in 1 BOX (50458-253-01) > 1 mL in 1 AMPULE |
NDC Code | 50458-253-01 |
Proprietary Name | Haldol Decanoate |
Package Description | 10 AMPULE in 1 BOX (50458-253-01) > 1 mL in 1 AMPULE |
Product NDC | 50458-253 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Haloperidol Decanoate |
Dosage Form Name | INJECTION |
Route Name | INTRAMUSCULAR |
Start Marketing Date | 19860114 |
Marketing Category Name | NDA |
Labeler Name | Janssen Pharmaceuticals, Inc. |
Substance Name | HALOPERIDOL DECANOATE |
Strength Number | 50 |
Strength Unit | mg/mL |
Pharmaceutical Classes | Typical Antipsychotic [EPC] |