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Metoclopramide
Metoclopramide - 51079-629-20 - (Metoclopramide)
Drug Information of Metoclopramide
| Product NDC: | 51079-629 |
| Proprietary Name: | Metoclopramide |
| Non Proprietary Name: | Metoclopramide |
| Active Ingredient(s): | 5 mg/1 & nbsp; Metoclopramide |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Metoclopramide
| Product NDC: | 51079-629 |
| Labeler Name: | UDL Laboratories, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA072801 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20110823 |
Package Information of Metoclopramide
| Package NDC: | 51079-629-20 |
| Package Description: | 100 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-629-20) > 1 TABLET in 1 BLISTER PACK (51079-629-01) |
NDC Information of Metoclopramide
| NDC Code | 51079-629-20 |
| Proprietary Name | Metoclopramide |
| Package Description | 100 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-629-20) > 1 TABLET in 1 BLISTER PACK (51079-629-01) |
| Product NDC | 51079-629 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Metoclopramide |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20110823 |
| Marketing Category Name | ANDA |
| Labeler Name | UDL Laboratories, Inc. |
| Substance Name | METOCLOPRAMIDE HYDROCHLORIDE |
| Strength Number | 5 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Dopamine D2 Antagonists [MoA],Dopamine-2 Receptor Antagonist [EPC] |
