Metoclopramide 00093-2204
Product NDC
00093-2204- Manufacturer
- Teva Pharmaceuticals Usa, Inc.
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- July 1, 1993
- Listing Expires
- December 31, 2027
- Application
- ANDA072801
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Metoclopramide Hydrochloride | 5 mg/1 |
Drug Class
Dopamine D2 Antagonists [MoA]Dopamine-2 Receptor Antagonist [EPC]
Packaging Options(2)
100 TABLET in 1 BOTTLE (0093-2204-01)
500 TABLET in 1 BOTTLE (0093-2204-05)