Product NDC: | 62559-1106 |
Proprietary Name: | Metoclopramide |
Non Proprietary Name: | Metoclopramide Hydrochloride |
Active Ingredient(s): | 5 mg/5mL & nbsp; Metoclopramide Hydrochloride |
Administration Route(s): | ORAL |
Dosage Form(s): | SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 62559-1106 |
Labeler Name: | ANIP Acquisition Company |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA071402 |
Marketing Category: | ANDA |
Start Marketing Date: | 20110310 |
Package NDC: | 62559-1106-6 |
Package Description: | 473 mL in 1 BOTTLE (62559-1106-6) |
NDC Code | 62559-1106-6 |
Proprietary Name | Metoclopramide |
Package Description | 473 mL in 1 BOTTLE (62559-1106-6) |
Product NDC | 62559-1106 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Metoclopramide Hydrochloride |
Dosage Form Name | SOLUTION |
Route Name | ORAL |
Start Marketing Date | 20110310 |
Marketing Category Name | ANDA |
Labeler Name | ANIP Acquisition Company |
Substance Name | METOCLOPRAMIDE HYDROCHLORIDE |
Strength Number | 5 |
Strength Unit | mg/5mL |
Pharmaceutical Classes | Dopamine D2 Antagonists [MoA],Dopamine-2 Receptor Antagonist [EPC] |