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Metoclopramide
Metoclopramide - 52584-450-39 - (Metoclopramide Hydrochloride)
Drug Information of Metoclopramide
| Product NDC: | 52584-450 |
| Proprietary Name: | Metoclopramide |
| Non Proprietary Name: | Metoclopramide Hydrochloride |
| Active Ingredient(s): | 10 mg/2mL & nbsp; Metoclopramide Hydrochloride |
| Administration Route(s): | INTRAMUSCULAR; INTRAVENOUS |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Metoclopramide
| Product NDC: | 52584-450 |
| Labeler Name: | General Injectables & Vaccines, Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA017862 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20100801 |
Package Information of Metoclopramide
| Package NDC: | 52584-450-39 |
| Package Description: | 1 VIAL, SINGLE-DOSE in 1 BAG (52584-450-39) > 2 mL in 1 VIAL, SINGLE-DOSE |
NDC Information of Metoclopramide
| NDC Code | 52584-450-39 |
| Proprietary Name | Metoclopramide |
| Package Description | 1 VIAL, SINGLE-DOSE in 1 BAG (52584-450-39) > 2 mL in 1 VIAL, SINGLE-DOSE |
| Product NDC | 52584-450 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Metoclopramide Hydrochloride |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRAMUSCULAR; INTRAVENOUS |
| Start Marketing Date | 20100801 |
| Marketing Category Name | NDA |
| Labeler Name | General Injectables & Vaccines, Inc |
| Substance Name | METOCLOPRAMIDE HYDROCHLORIDE |
| Strength Number | 10 |
| Strength Unit | mg/2mL |
| Pharmaceutical Classes | Dopamine D2 Antagonists [MoA],Dopamine-2 Receptor Antagonist [EPC] |
