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Haloperidol
Haloperidol - 49349-909-41 - (Haloperidol)
Drug Information of Haloperidol
| Product NDC: | 49349-909 |
| Proprietary Name: | Haloperidol |
| Non Proprietary Name: | Haloperidol |
| Active Ingredient(s): | 5 mg/1 & nbsp; Haloperidol |
| Administration Route(s): | INTRAMUSCULAR |
| Dosage Form(s): | INJECTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Haloperidol
| Product NDC: | 49349-909 |
| Labeler Name: | REMEDYREPACK INC. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA015923 |
| Marketing Category: | NDA AUTHORIZED GENERIC |
| Start Marketing Date: | 20130410 |
Package Information of Haloperidol
| Package NDC: | 49349-909-41 |
| Package Description: | 1 INJECTION in 1 VIAL (49349-909-41) |
NDC Information of Haloperidol
| NDC Code | 49349-909-41 |
| Proprietary Name | Haloperidol |
| Package Description | 1 INJECTION in 1 VIAL (49349-909-41) |
| Product NDC | 49349-909 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Haloperidol |
| Dosage Form Name | INJECTION |
| Route Name | INTRAMUSCULAR |
| Start Marketing Date | 20130410 |
| Marketing Category Name | NDA AUTHORIZED GENERIC |
| Labeler Name | REMEDYREPACK INC. |
| Substance Name | HALOPERIDOL |
| Strength Number | 5 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Typical Antipsychotic [EPC] |
