Metoclopramide
- Product NDC
- 67296-1738
- 11-digit product format
- 672961738
- Labeler code
- 67296
- Product ID
- 67296-1738_b3376023-de95-f7a8-e053-2995a90a4dcb
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metoclopramide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- RedPharm Drug, Inc.
- Application
- ANDA070581
- Marketing category
- ANDA
- Marketing start
- 2019-11-01
- Marketing end
- 0000-00-00
- 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
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 67296-1738-7 | Metoclopramide | 15 in 1 BOTTLE | TABLET | 15 | | 3 |
| 67296-1738-8 | Metoclopramide | 21 in 1 BOTTLE | TABLET | 21 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 67296-1738 | METOCLOPRAMIDE TABLET [REDPHARM DRUG, INC.] | 3 | Legacy NDC, 2 package rows | 20201104_972813e4-afbb-7c63-e053-2a95a90afef3.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 |
|---|
| 67296-1738-7 | 67296173807 | 15 TABLET in 1 BOTTLE (67296-1738-7) | 15 tablet | 2019-11-01 | 0000-00-00 | No | No | Current |
| 67296-1738-8 | 67296173808 | 21 TABLET in 1 BOTTLE (67296-1738-8) | 21 tablet | 2019-11-01 | 0000-00-00 | No | No | Current |