Metoclopramide
- Product NDC
- 71335-2732
- 11-digit product format
- 713352732
- Labeler code
- 71335
- Product ID
- 71335-2732_c671d4bb-5473-4613-a593-9aacd62577ee
- 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
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Metoclopramide
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| METOCLOPRAMIDE HYDROCHLORIDE | 5 mg/5mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | W1792A2RVD |
| Rxcui | 104884 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 71335-2732-1 | Metoclopramide | 473 mL in 1 BOTTLE, PLASTIC | SOLUTION | 473 | | 100 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 71335-2732-1 | 71335273201 | 473 mL in 1 BOTTLE, PLASTIC (71335-2732-1) | 473 ml | 2025-07-29 | No | No | Current |