Metoclopramide
- Product NDC
- 68788-7930
- 11-digit product format
- 687887930
- Labeler code
- 68788
- Product ID
- 68788-7930_47f3f4a8-595a-42f2-967f-958a7c8e9467
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metoclopramide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA070184
- Marketing category
- ANDA
- Marketing start
- 2021-06-15
- Substance
- METOCLOPRAMIDE HYDROCHLORIDE
- Active strength
- 10 mg/1
- 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 | 10 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | W1792A2RVD |
| Rxcui | 311666 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 68788-7930-3 | Metoclopramide | 30 in 1 BOTTLE | TABLET | 30 | | 5 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68788-7930 | METOCLOPRAMIDE TABLET [PREFERRED PHARMACEUTICALS INC.] | 4 | Current NDC, Legacy NDC, 1 package rows | 20240718_697ec7b1-945a-4a31-b585-f051dc246165.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68788-7930-3 | 68788793003 | 30 TABLET in 1 BOTTLE (68788-7930-3) | 30 tablet | 2021-06-15 | 0000-00-00 | No | No | Current |