| 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] |