NDC 71335-1259 – Metoclopramide
Metoclopramide Hydrochloride 5 mg/1 · Tablet · Oral
Product NDC71335-1259
Product details
- Brand name
- Metoclopramide
- Generic name
- Metoclopramide
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA072801
- Marketed since
- July 1, 1993
- Listing expires
- December 31, 2026
- Pharmacologic class
- Dopamine-2 Receptor Antagonist
Active ingredients
- Metoclopramide Hydrochloride 5 mg/1
Uses, dosage, side effects and warnings for Metoclopramide →
Package NDC codes (5)
| Package NDC | Description | Since |
|---|---|---|
| 71335-1259-1 | 30 TABLET in 1 BOTTLE (71335-1259-1) | May 24, 2024 |
| 71335-1259-2 | 120 TABLET in 1 BOTTLE (71335-1259-2) | May 24, 2024 |
| 71335-1259-3 | 90 TABLET in 1 BOTTLE (71335-1259-3) | May 24, 2024 |
| 71335-1259-4 | 60 TABLET in 1 BOTTLE (71335-1259-4) | May 24, 2024 |
| 71335-1259-5 | 100 TABLET in 1 BOTTLE (71335-1259-5) | May 24, 2024 |
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