Product NDC: | 0093-9604 |
Proprietary Name: | Haloperidol |
Non Proprietary Name: | Haloperidol lactate |
Active Ingredient(s): | 2 mg/mL & nbsp; Haloperidol lactate |
Administration Route(s): | ORAL |
Dosage Form(s): | SOLUTION, CONCENTRATE |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0093-9604 |
Labeler Name: | Teva Pharmaceuticals USA Inc |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA071617 |
Marketing Category: | ANDA |
Start Marketing Date: | 19881201 |
Package NDC: | 0093-9604-12 |
Package Description: | 120 mL in 1 BOTTLE, DROPPER (0093-9604-12) |
NDC Code | 0093-9604-12 |
Proprietary Name | Haloperidol |
Package Description | 120 mL in 1 BOTTLE, DROPPER (0093-9604-12) |
Product NDC | 0093-9604 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Haloperidol lactate |
Dosage Form Name | SOLUTION, CONCENTRATE |
Route Name | ORAL |
Start Marketing Date | 19881201 |
Marketing Category Name | ANDA |
Labeler Name | Teva Pharmaceuticals USA Inc |
Substance Name | HALOPERIDOL LACTATE |
Strength Number | 2 |
Strength Unit | mg/mL |
Pharmaceutical Classes | Typical Antipsychotic [EPC] |