Metoclopramide

Metoclopramide 10mg

Approved

Approval ID

972813e4-afbb-7c63-e053-2a95a90afef3

Product Type

HUMAN PRESCRIPTION DRUG LABEL

Effective Date

Nov 3, 2020

Manufacturers

FDA

RedPharm Drug, Inc.

DUNS: 828374897

Products 1

Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.

NDC Product Code67296-1738

Application NumberANDA070581

Marketing CategoryC73584

Route of AdministrationORAL

Effective DateNovember 3, 2020

Generic NameMetoclopramide

SILICON DIOXIDEInactive

Code: ETJ7Z6XBU4

Classification: IACT

STARCH, CORNInactive

Code: O8232NY3SJ

Classification: IACT

MAGNESIUM STEARATEInactive

Code: 70097M6I30

Classification: IACT

MANNITOLInactive

Code: 3OWL53L36A

Classification: IACT

METOCLOPRAMIDE HYDROCHLORIDEActive

Quantity: 10 mg in 1 1

Code: W1792A2RVD

Classification: ACTIM