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Metoclopramide hydrochloride
Metoclopramide hydrochloride - 0703-4502-04 - (Metoclopramide hydrochloride)
Drug Information of Metoclopramide hydrochloride
| Product NDC: | 0703-4502 |
| Proprietary Name: | Metoclopramide hydrochloride |
| Non Proprietary Name: | Metoclopramide hydrochloride |
| Active Ingredient(s): | 5 mg/mL & nbsp; Metoclopramide hydrochloride |
| Administration Route(s): | INTRAMUSCULAR; INTRAVENOUS |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Metoclopramide hydrochloride
| Product NDC: | 0703-4502 |
| Labeler Name: | Teva Parenteral Medicines, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA073135 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19911201 |
Package Information of Metoclopramide hydrochloride
| Package NDC: | 0703-4502-04 |
| Package Description: | 25 VIAL, SINGLE-DOSE in 1 TRAY (0703-4502-04) > 2 mL in 1 VIAL, SINGLE-DOSE (0703-4502-01) |
NDC Information of Metoclopramide hydrochloride
| NDC Code | 0703-4502-04 |
| Proprietary Name | Metoclopramide hydrochloride |
| Package Description | 25 VIAL, SINGLE-DOSE in 1 TRAY (0703-4502-04) > 2 mL in 1 VIAL, SINGLE-DOSE (0703-4502-01) |
| Product NDC | 0703-4502 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Metoclopramide hydrochloride |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRAMUSCULAR; INTRAVENOUS |
| Start Marketing Date | 19911201 |
| Marketing Category Name | ANDA |
| Labeler Name | Teva Parenteral Medicines, Inc. |
| Substance Name | METOCLOPRAMIDE HYDROCHLORIDE |
| Strength Number | 5 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Dopamine D2 Antagonists [MoA],Dopamine-2 Receptor Antagonist [EPC] |
