Metoclopramide
- Product NDC
- 68071-3924
- 11-digit product format
- 680713924
- Labeler code
- 68071
- Product ID
- 68071-3924_45251536-a1a6-b87d-e063-6294a90a76ed
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metoclopramide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NuCare Pharamceuticals, Inc.
- Application
- ANDA072215
- Marketing category
- ANDA
- Marketing start
- 2025-02-12
- 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
- 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/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 |
|---|
| 68071-3924-3 | Metoclopramide | 30 in 1 BOTTLE | TABLET | 30 | | 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 |
|---|
| 68071-3924-3 | 68071392403 | 30 TABLET in 1 BOTTLE (68071-3924-3) | 30 tablet | 2025-12-04 | No | No | Current |