Metoclopramide
METOCLOPRAMIDE TABLETS, USP
Approved
Approval ID
673da5be-439b-b22c-e053-2a91aa0a0008
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Mar 3, 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
NDC Product Code68071-4326
Application NumberANDA070581
Marketing CategoryC73584
Route of AdministrationORAL
Effective DateMarch 3, 2021
Generic NameMetoclopramide
INGREDIENTS (5)
SILICON DIOXIDEInactive
Code: ETJ7Z6XBU4
Classification: IACT
MANNITOLInactive
Code: 3OWL53L36A
Classification: IACT
STARCH, CORNInactive
Code: O8232NY3SJ
Classification: IACT
MAGNESIUM STEARATEInactive
Code: 70097M6I30
Classification: IACT
METOCLOPRAMIDE HYDROCHLORIDEActive
Quantity: 10 mg in 1 1
Code: W1792A2RVD
Classification: ACTIM