Product NDC: | 0409-1187 |
Proprietary Name: | Droperidol |
Non Proprietary Name: | DROPERIDOL |
Active Ingredient(s): | 2.5 mg/mL & nbsp; DROPERIDOL |
Administration Route(s): | INTRAMUSCULAR; INTRAVENOUS |
Dosage Form(s): | INJECTION, SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0409-1187 |
Labeler Name: | Hospira, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA071981 |
Marketing Category: | ANDA |
Start Marketing Date: | 20110811 |
Package NDC: | 0409-1187-01 |
Package Description: | 10 AMPULE in 1 CARTON (0409-1187-01) > 2 mL in 1 AMPULE |
NDC Code | 0409-1187-01 |
Proprietary Name | Droperidol |
Package Description | 10 AMPULE in 1 CARTON (0409-1187-01) > 2 mL in 1 AMPULE |
Product NDC | 0409-1187 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | DROPERIDOL |
Dosage Form Name | INJECTION, SOLUTION |
Route Name | INTRAMUSCULAR; INTRAVENOUS |
Start Marketing Date | 20110811 |
Marketing Category Name | ANDA |
Labeler Name | Hospira, Inc. |
Substance Name | DROPERIDOL |
Strength Number | 2.5 |
Strength Unit | mg/mL |
Pharmaceutical Classes | Dopamine D2 Antagonists [MoA],Dopamine-2 Receptor Antagonist [EPC] |