Metoclopramide
- Product NDC
- 70518-0617
- 11-digit product format
- 705180617
- Labeler code
- 70518
- Product ID
- 70518-0617_8643d513-86dc-cea3-e053-2991aa0a0ddd
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metoclopramide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA070581
- Marketing category
- ANDA
- Marketing start
- 2017-07-12
- 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