United States · FDA National Drug Code directory
Metoclopramide
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 17856-1190_3ce771f8-a078-c4ca-e063-6294a90ae2b2
- Product NDC
- 17856-1190
- Form
- SOLUTION
- Composition / generic term
- Metoclopramide
- Labeler
- ATLANTIC BIOLOGICALS CORP.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20150518
- Source listing expiry
- 20261231
Source-listed ingredients
- METOCLOPRAMIDE HYDROCHLORIDE — 5 mg/5mL
These values do not establish equivalence or a dose recommendation.
Packages
- 72 CUP, UNIT-DOSE in 1 CASE (17856-1190-1) / 5 mL in 1 CUP, UNIT-DOSE · 17856-1190-1
- 120 SYRINGE in 1 CASE (17856-1190-2) / 1 mL in 1 SYRINGE · 17856-1190-2
Source and coverage
Open FDA National Drug Code directory →
Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
Browse United States records →