Metoclopramide
- Product NDC
- 49999-758
- 11-digit product format
- 499990758
- Labeler code
- 49999
- Product ID
- 49999-758_40db2e99-1d21-4df4-bf80-ab14eaacc6f0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metoclopramide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Lake Erie Medical DBA Quality Care Products LLC
- Application
- ANDA072801
- Marketing category
- ANDA
- Marketing start
- 1993-07-01
- Marketing end
- 0000-00-00
- 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
- 2019-12-31
- Current FDA listing
- Historical FDA.report record