Metoclopramide
- Product NDC
- 68788-0430
- 11-digit product format
- 687880430
- Labeler code
- 68788
- Product ID
- 68788-0430_bf0b84c1-6ad7-4269-b362-2375b24859b3
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metoclopramide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals, Inc.
- Application
- ANDA070184
- Marketing category
- ANDA
- Marketing start
- 2013-04-01
- 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
- 2020-12-31
- Current FDA listing
- Historical FDA.report record