| NDC Code | 0615-8071-39 |
|---|
| Package Description | 30 TABLET in 1 BLISTER PACK (0615-8071-39) |
|---|
| Product NDC | 0615-8071 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Metoclopramide Hydrochloride |
|---|
| Non-Proprietary Name | Metoclopramide Hydrochloride |
|---|
| Dosage Form | TABLET |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20110822 |
|---|
| End Marketing Date | 20201231 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA071250 |
|---|
| Manufacturer | NCS HealthCare of KY, Inc dba Vangard Labs |
|---|
| Substance Name | METOCLOPRAMIDE HYDROCHLORIDE |
|---|
| Strength | 10 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Dopamine D2 Antagonists [MoA],Dopamine-2 Receptor Antagonist [EPC] |
|---|