Metoclopramide
- Product NDC
- 68788-7226
- 11-digit product format
- 687887226
- Labeler code
- 68788
- Product ID
- 68788-7226_25f7d41c-f58b-4623-99fe-6355598be96e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metoclopramide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA070581
- Marketing category
- ANDA
- Marketing start
- 2018-08-07
- Marketing end
- 2023-10-30
- 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
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68788-7226-3 | 68788722603 | 30 TABLET in 1 BOTTLE (68788-7226-3) | 30 tablet | 2018-08-07 | 0000-00-00 | No | No | Current |