Metoclopramide
- Product NDC
- 70518-0669
- 11-digit product format
- 705180669
- Labeler code
- 70518
- Product ID
- 70518-0669_522da090-b1c9-b1fa-e063-6394a90a466a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metoclopramide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA070184
- Marketing category
- ANDA
- Marketing start
- 2019-08-14
- 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
- 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 | 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 |
|---|
| 70518-0669-0 | Metoclopramide | 30 in 1 BLISTER PACK | TABLET | 30 | | 15 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70518-0669 | METOCLOPRAMIDE TABLET [REMEDYREPACK INC.] | 12 | Current NDC, Legacy NDC, 1 package rows | 20250429_6637cb78-d50a-4dbf-8fb7-b1b5102c5c5f.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 |
|---|
| 70518-0669-0 | 70518066900 | 30 TABLET in 1 BLISTER PACK (70518-0669-0) | 30 tablet | 2019-08-14 | 0000-00-00 | No | No | Current |