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Metoclopramide
Metoclopramide - 0121-1576-10 - (Metoclopramide Hydrochloride)
Drug Information of Metoclopramide
| Product NDC: | 0121-1576 |
| Proprietary Name: | Metoclopramide |
| Non Proprietary Name: | Metoclopramide Hydrochloride |
| Active Ingredient(s): | 5 mg/5mL & nbsp; Metoclopramide Hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Metoclopramide
| Product NDC: | 0121-1576 |
| Labeler Name: | Pharmaceutical Associates, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA072744 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19910601 |
Package Information of Metoclopramide
| Package NDC: | 0121-1576-10 |
| Package Description: | 10 TRAY in 1 CASE (0121-1576-10) > 10 CUP, UNIT-DOSE in 1 TRAY > 10 mL in 1 CUP, UNIT-DOSE |
NDC Information of Metoclopramide
| NDC Code | 0121-1576-10 |
| Proprietary Name | Metoclopramide |
| Package Description | 10 TRAY in 1 CASE (0121-1576-10) > 10 CUP, UNIT-DOSE in 1 TRAY > 10 mL in 1 CUP, UNIT-DOSE |
| Product NDC | 0121-1576 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Metoclopramide Hydrochloride |
| Dosage Form Name | SOLUTION |
| Route Name | ORAL |
| Start Marketing Date | 19910601 |
| Marketing Category Name | ANDA |
| Labeler Name | Pharmaceutical Associates, Inc. |
| Substance Name | METOCLOPRAMIDE HYDROCHLORIDE |
| Strength Number | 5 |
| Strength Unit | mg/5mL |
| Pharmaceutical Classes | Dopamine D2 Antagonists [MoA],Dopamine-2 Receptor Antagonist [EPC] |
