Metoclopramide
METOCLOPRAMIDE TABLETS, USP
Approved
Approval ID
76513627-0960-e049-e053-2a91aa0aa7d2
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Feb 22, 2021
Manufacturers
FDA
NuCare Pharmaceuticals,Inc.
DUNS: 010632300
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
Metoclopramide
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code68071-4569
Application NumberANDA070581
Product Classification
M
Marketing Category
C73584
G
Generic Name
Metoclopramide
Product Specifications
Route of AdministrationORAL
Effective DateFebruary 22, 2021
FDA Product Classification
INGREDIENTS (5)
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