Metoclopramide
- Product NDC
- 67296-2213
- 11-digit product format
- 672962213
- Labeler code
- 67296
- Product ID
- 67296-2213_49eb7254-b7f9-6119-e063-6394a90aaf3d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metoclopramide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Redpharm Drug
- Application
- NDA017854
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2021-12-13
- Substance
- METOCLOPRAMIDE HYDROCHLORIDE
- Active strength
- 5 mg/1
- Pharmacologic classes
- Dopamine D2 Antagonists [MoA], Dopamine-2 Receptor Antagonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Metoclopramide
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| METOCLOPRAMIDE HYDROCHLORIDE | 5 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | W1792A2RVD |
| Rxcui | 311668 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 67296-2213-1 | Metoclopramide | 15 in 1 BOTTLE, PLASTIC | TABLET | 15 | | 1 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 67296-2213-1 | 67296221301 | 15 TABLET in 1 BOTTLE, PLASTIC (67296-2213-1) | 15 tablet | 2021-12-13 | No | No | Historical |