Metoclopramide
- Product NDC
- 71335-2997
- 11-digit product format
- 713352997
- Labeler code
- 71335
- Product ID
- 71335-2997_1ebf7183-a979-4334-9621-b918f50a1ea4
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metoclopramide
- Dosage form
- SOLUTION
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA071402
- Marketing category
- ANDA
- Marketing start
- 2015-05-18
- Substance
- METOCLOPRAMIDE HYDROCHLORIDE
- Active strength
- 5 mg/5mL
- Pharmacologic classes
- Dopamine D2 Antagonists [MoA], Dopamine-2 Receptor Antagonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| W1792A2RVD | METOCLOPRAMIDE HYDROCHLORIDE | 54143-57-6 | METOCLOPRAMIDE HYDROCHLORIDE |
| L4YEB44I46 | METOCLOPRAMIDE | 364-62-5 | Metoclopramide |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 71335-2997-1 | 71335299701 | 473 mL in 1 BOTTLE (71335-2997-1) | 473 ml | 2025-11-05 | No | No | Historical |