NDC 0703-4502

Metoclopramide

Metoclopramide

Metoclopramide is a Intramuscular; Intravenous Injection, Solution in the Human Prescription Drug category. It is labeled and distributed by Teva Parenteral Medicines, Inc.. The primary component is Metoclopramide Hydrochloride.

Product ID0703-4502_0519e705-4235-4590-8cb4-0dd694241c78
NDC0703-4502
Product TypeHuman Prescription Drug
Proprietary NameMetoclopramide
Generic NameMetoclopramide
Dosage FormInjection, Solution
Route of AdministrationINTRAMUSCULAR; INTRAVENOUS
Marketing Start Date2015-02-09
Marketing End Date2020-07-31
Marketing CategoryANDA / ANDA
Application NumberANDA073135
Labeler NameTeva Parenteral Medicines, Inc.
Substance NameMETOCLOPRAMIDE HYDROCHLORIDE
Active Ingredient Strength5 mg/mL
Pharm ClassesDopamine D2 Antagonists [MoA],Dopamine-2 Receptor Antagonist [EPC]
NDC Exclude FlagN

Packaging

NDC 0703-4502-84

25 VIAL, SINGLE-USE in 1 TRAY (0703-4502-84) > 2 mL in 1 VIAL, SINGLE-USE (0703-4502-81)
Marketing Start Date2015-08-17
Marketing End Date2021-03-31
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 0703-4502-94 [00703450294]

Metoclopramide INJECTION, SOLUTION
Marketing CategoryANDA
Application NumberANDA073135
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitML
Marketing Start Date2015-02-09
Marketing End Date2020-07-31

NDC 0703-4502-81 [00703450281]

Metoclopramide INJECTION, SOLUTION
Marketing CategoryANDA
Application NumberANDA073135
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitML
Marketing Start Date2015-08-17
Marketing End Date2021-03-31

NDC 0703-4502-01 [00703450201]

Metoclopramide INJECTION, SOLUTION
Marketing CategoryANDA
Application NumberANDA073135
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitML
Marketing Start Date1991-12-01

NDC 0703-4502-04 [00703450204]

Metoclopramide INJECTION, SOLUTION
Marketing CategoryANDA
Application NumberANDA073135
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitML
Marketing Start Date1991-12-01

NDC 0703-4502-91 [00703450291]

Metoclopramide INJECTION, SOLUTION
Marketing CategoryANDA
Application NumberANDA073135
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitML
Marketing Start Date2015-02-09
Marketing End Date2020-07-31

NDC 0703-4502-84 [00703450284]

Metoclopramide INJECTION, SOLUTION
Marketing CategoryANDA
Application NumberANDA073135
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitML
Marketing Start Date2015-08-17
Marketing End Date2021-03-31

Drug Details

Active Ingredients

IngredientStrength
METOCLOPRAMIDE HYDROCHLORIDE5 mg/mL

OpenFDA Data

SPL SET ID:f18e7463-4497-4d0a-a6f9-c272cba6600c
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 311670

    • Pharmacological Class

    • Dopamine D2 Antagonists [MoA]
    • Dopamine-2 Receptor Antagonist [EPC]
    • Dopamine D2 Antagonists [MoA]
    • Dopamine-2 Receptor Antagonist [EPC]

    NDC Crossover Matching brand name "Metoclopramide" or generic name "Metoclopramide"

    NDCBrand NameGeneric Name
    0093-2203MetoclopramideMetoclopramide
    0093-2204MetoclopramideMetoclopramide
    0121-0576Metoclopramidemetoclopramide hydrochloride
    0121-1576Metoclopramidemetoclopramide hydrochloride
    0404-9910MetoclopramideMetoclopramide Hydrochloride
    0409-3414Metoclopramidemetoclopramide
    0409-5255Metoclopramidemetoclopramide
    0440-1771MetoclopramideMetoclopramide
    0615-2536MetoclopramideMetoclopramide
    0615-7698MetoclopramideMetoclopramide
    0615-7752MetoclopramideMetoclopramide
    0615-7932MetoclopramideMetoclopramide
    0615-8285MetoclopramideMetoclopramide
    0703-4502MetoclopramideMetoclopramide
    12634-112MetoclopramideMetoclopramide
    17856-0537Metoclopramidemetoclopramide hydrochloride
    17856-0576Metoclopramidemetoclopramide hydrochloride
    17856-3727Metoclopramidemetoclopramide hydrochloride
    21695-346MetoclopramideMetoclopramide
    21695-485MetoclopramideMetoclopramide
    23155-240MetoclopramideMetoclopramide Hydrochloride
    68071-4326MetoclopramideMetoclopramide
    68071-4569MetoclopramideMetoclopramide
    68084-676MetoclopramideMetoclopramide
    68151-1741MetoclopramideMetoclopramide
    68788-0430MetoclopramideMetoclopramide
    68788-7226MetoclopramideMetoclopramide
    68788-9093MetoclopramideMetoclopramide
    70518-0669MetoclopramideMetoclopramide
    70518-0617MetoclopramideMetoclopramide
    70518-1193MetoclopramideMetoclopramide
    71335-0790MetoclopramideMetoclopramide
    71335-0362MetoclopramideMetoclopramide
    71872-7076MetoclopramideMetoclopramide
    71872-7075MetoclopramideMetoclopramide
    76045-101MetoclopramideMetoclopramide
    33261-166MetoclopramideMetoclopramide
    42291-595MetoclopramideMetoclopramide
    42291-596MetoclopramideMetoclopramide
    43353-274MetoclopramideMetoclopramide
    49884-689MetoclopramideMetoclopramide
    49999-057MetoclopramideMetoclopramide
    49999-758MetoclopramideMetoclopramide
    50090-2221MetoclopramideMetoclopramide
    50436-1873MetoclopramideMetoclopramide
    50436-0576MetoclopramideMetoclopramide
    51079-886MetoclopramideMetoclopramide
    51079-888MetoclopramideMetoclopramide
    51662-1288METOCLOPRAMIDEMETOCLOPRAMIDE
    52584-414MetoclopramideMetoclopramide
    © 2024 FDA.report
    This site is not affiliated with or endorsed by the FDA.