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Reglan
Reglan - 0091-6701-63 - (metoclopramide hydrochloride)
Drug Information of Reglan
| Product NDC: | 0091-6701 |
| Proprietary Name: | Reglan |
| Non Proprietary Name: | metoclopramide hydrochloride |
| Active Ingredient(s): | 10 mg/1 & nbsp; metoclopramide hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Reglan
| Product NDC: | 0091-6701 |
| Labeler Name: | UCB, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA017854 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20030505 |
Package Information of Reglan
| Package NDC: | 0091-6701-63 |
| Package Description: | 100 TABLET in 1 BOTTLE (0091-6701-63) |
NDC Information of Reglan
| NDC Code | 0091-6701-63 |
| Proprietary Name | Reglan |
| Package Description | 100 TABLET in 1 BOTTLE (0091-6701-63) |
| Product NDC | 0091-6701 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | metoclopramide hydrochloride |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20030505 |
| Marketing Category Name | NDA |
| Labeler Name | UCB, Inc. |
| Substance Name | METOCLOPRAMIDE HYDROCHLORIDE |
| Strength Number | 10 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Dopamine D2 Antagonists [MoA],Dopamine-2 Receptor Antagonist [EPC] |
