NDC 0093-2203 – Metoclopramide
Metoclopramide Hydrochloride 10 mg/1 · Tablet · Oral
Product NDC0093-2203
Product details
- Brand name
- Metoclopramide
- Generic name
- Metoclopramide
- Labeler
- Teva Pharmaceuticals USA, Inc.
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA070184
- Marketed since
- September 30, 1990
- Listing expires
- December 31, 2027
- Pharmacologic class
- Dopamine-2 Receptor Antagonist
Active ingredients
- Metoclopramide Hydrochloride 10 mg/1
Uses, dosage, side effects and warnings for Metoclopramide →
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 0093-2203-01 | 100 TABLET in 1 BOTTLE (0093-2203-01) | Sep 30, 1990 |
| 0093-2203-05 | 500 TABLET in 1 BOTTLE (0093-2203-05) | Sep 30, 1990 |
| 0093-2203-10 | 1000 TABLET in 1 BOTTLE (0093-2203-10) | Sep 30, 1990 |
Recalls mentioning this NDC
- D-0473-2025 Jul 2, 2025 · Class II
Presence of foreign tablets/capsules.
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