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Haloperidol
Haloperidol - 63323-474-10 - (HALOPERIDOL LACTATE)
Drug Information of Haloperidol
| Product NDC: | 63323-474 |
| Proprietary Name: | Haloperidol |
| Non Proprietary Name: | HALOPERIDOL LACTATE |
| Active Ingredient(s): | 5 mg/mL & nbsp; HALOPERIDOL LACTATE |
| Administration Route(s): | INTRAMUSCULAR |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Haloperidol
| Product NDC: | 63323-474 |
| Labeler Name: | APP Pharmaceuticals, LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA075689 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20110328 |
Package Information of Haloperidol
| Package NDC: | 63323-474-10 |
| Package Description: | 1 VIAL, MULTI-DOSE in 1 BOX (63323-474-10) > 10 mL in 1 VIAL, MULTI-DOSE |
NDC Information of Haloperidol
| NDC Code | 63323-474-10 |
| Proprietary Name | Haloperidol |
| Package Description | 1 VIAL, MULTI-DOSE in 1 BOX (63323-474-10) > 10 mL in 1 VIAL, MULTI-DOSE |
| Product NDC | 63323-474 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | HALOPERIDOL LACTATE |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRAMUSCULAR |
| Start Marketing Date | 20110328 |
| Marketing Category Name | ANDA |
| Labeler Name | APP Pharmaceuticals, LLC |
| Substance Name | HALOPERIDOL LACTATE |
| Strength Number | 5 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Typical Antipsychotic [EPC] |
