Metoclopramide 5 solution

Metoclopramide (Morton Grove Pharmaceuticals), manufactured drug form of Metoclopramide hydrochloride, 5mg/5mL metoclopramide hydrochloride solution, NDC 60432-622

Available in:

NDC Product ID:

  • 60432-622

Manufacturer:

Manufactured drug form

Manufactured form of:

Generic drug:

  • Yes

Label date:

  • Feb 25, 2011

Label link:

Label sections:

Section name Section URI Prominent warning Highlight text Section LOINC code
  • Spl Unclassified Section
  • No
  • 42229-5
  • Warning: Tardive Dyskinesia
  • Yes
  • Treatment with metoclopramide can cause tardive dyskinesia, a serious movement disorder that is often irreversible. The risk of developing tardive dyskinesia increases with duration of treatment and total cumulative dose. Metoclopramide therapy should be discontinued in patients who develop signs or symptoms of tardive dyskinesia. There is no known treatment for tardive dyskinesia. In some patients, symptoms may lessen or resolve after metoclopramide treatment is stopped. Treatment with metoclopramide for longer than 12 weeks should be avoided in all but rare cases where therapeutic benefit is thought to outweigh the risk of developing tardive dyskinesia. See WARNINGS
  • 34066-1
  • Description
  • No
  • 34089-3
  • Clinical Pharmacology
  • No
  • 34090-1
  • Indications And Usage
  • No
  • 34067-9
  • Contraindications
  • No
  • 34070-3
  • Warnings
  • No
  • 34071-1
  • Precautions
  • No
  • 42232-9
  • Adverse Reactions
  • No
  • 34084-4
  • Overdosage
  • No
  • 34088-5
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Discontinued:

  • No

Marketing start date:

  • Apr 5, 1995

FDA application number:

  • ANDA074703

Color:

Flavor:

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