NDC Code | 68071-4551-8 |
Package Description | 8 TABLET in 1 BOTTLE (68071-4551-8) |
Product NDC | 68071-4551 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Metoclopramide Hydrochloride |
Non-Proprietary Name | Metoclopramide Hydrochloride |
Dosage Form | TABLET |
Usage | ORAL |
Start Marketing Date | 20110822 |
Marketing Category Name | ANDA |
Application Number | ANDA072750 |
Manufacturer | NuCare Pharmaceuticals,Inc. |
Substance Name | METOCLOPRAMIDE HYDROCHLORIDE |
Strength | 5 |
Strength Unit | mg/1 |
Pharmacy Classes | Dopamine D2 Antagonists [MoA], Dopamine-2 Receptor Antagonist [EPC] |