Product NDC: | 0615-7752 |
Proprietary Name: | Metoclopramide |
Non Proprietary Name: | Metoclopramide |
Active Ingredient(s): | 10 mg/1 & nbsp; Metoclopramide |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0615-7752 |
Labeler Name: | NCS HealthCare of KY, Inc dba Vangard Labs |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA070581 |
Marketing Category: | ANDA |
Start Marketing Date: | 19851017 |
Package NDC: | 0615-7752-31 |
Package Description: | 31 TABLET in 1 BLISTER PACK (0615-7752-31) |
NDC Code | 0615-7752-31 |
Proprietary Name | Metoclopramide |
Package Description | 31 TABLET in 1 BLISTER PACK (0615-7752-31) |
Product NDC | 0615-7752 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Metoclopramide |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 19851017 |
Marketing Category Name | ANDA |
Labeler Name | NCS HealthCare of KY, Inc dba Vangard Labs |
Substance Name | METOCLOPRAMIDE HYDROCHLORIDE |
Strength Number | 10 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Dopamine D2 Antagonists [MoA],Dopamine-2 Receptor Antagonist [EPC] |