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METOZOLV
METOZOLV - 65649-432-02 - (METOCLOPRAMIDE HYDROCHLORIDE)
Drug Information of METOZOLV
| Product NDC: | 65649-432 |
| Proprietary Name: | METOZOLV |
| Non Proprietary Name: | METOCLOPRAMIDE HYDROCHLORIDE |
| Active Ingredient(s): | 10 mg/1 & nbsp; METOCLOPRAMIDE HYDROCHLORIDE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, ORALLY DISINTEGRATING |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of METOZOLV
| Product NDC: | 65649-432 |
| Labeler Name: | Salix Pharmaceuticals, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA022246 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20090904 |
Package Information of METOZOLV
| Package NDC: | 65649-432-02 |
| Package Description: | 10 BLISTER PACK in 1 CARTON (65649-432-02) > 10 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK |
NDC Information of METOZOLV
| NDC Code | 65649-432-02 |
| Proprietary Name | METOZOLV |
| Package Description | 10 BLISTER PACK in 1 CARTON (65649-432-02) > 10 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK |
| Product NDC | 65649-432 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | METOCLOPRAMIDE HYDROCHLORIDE |
| Dosage Form Name | TABLET, ORALLY DISINTEGRATING |
| Route Name | ORAL |
| Start Marketing Date | 20090904 |
| Marketing Category Name | NDA |
| Labeler Name | Salix Pharmaceuticals, Inc. |
| Substance Name | METOCLOPRAMIDE HYDROCHLORIDE |
| Strength Number | 10 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Dopamine D2 Antagonists [MoA],Dopamine-2 Receptor Antagonist [EPC] |
