Product NDC: | 16714-061 |
Proprietary Name: | Metoclopramide Hydrochloride |
Non Proprietary Name: | Metoclopramide Hydrochloride |
Active Ingredient(s): | 5 mg/1 & nbsp; Metoclopramide Hydrochloride |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 16714-061 |
Labeler Name: | Northstar RxLLC |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA078374 |
Marketing Category: | ANDA |
Start Marketing Date: | 20110317 |
Package NDC: | 16714-061-03 |
Package Description: | 90 TABLET in 1 BOTTLE (16714-061-03) |
NDC Code | 16714-061-03 |
Proprietary Name | Metoclopramide Hydrochloride |
Package Description | 90 TABLET in 1 BOTTLE (16714-061-03) |
Product NDC | 16714-061 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Metoclopramide Hydrochloride |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 20110317 |
Marketing Category Name | ANDA |
Labeler Name | Northstar RxLLC |
Substance Name | METOCLOPRAMIDE HYDROCHLORIDE |
Strength Number | 5 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Dopamine D2 Antagonists [MoA],Dopamine-2 Receptor Antagonist [EPC] |