Metoclopramide Hydrochloride
- Product NDC
- 68788-6791
- 11-digit product format
- 687886791
- Labeler code
- 68788
- Product ID
- 68788-6791_3215df94-230a-4d18-9a45-4ba08f196add
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metoclopramide Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals, Inc.
- Application
- ANDA071250
- Marketing category
- ANDA
- Marketing start
- 2016-11-02
- 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
- 2022-12-31
- 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 |
|---|
| 68788-6791-3 | 68788679103 | 30 TABLET in 1 BOTTLE, PLASTIC (68788-6791-3) | 30 tablet | 2016-11-02 | 0000-00-00 | No | No | Current |