metoclopramide

Generic: metoclopramide

Labeler: northwind health company, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name metoclopramide
Generic Name metoclopramide
Labeler northwind health company, llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

metoclopramide hydrochloride 10 mg/1

Manufacturer
Northwind Health Company, LLC

Identifiers & Regulatory

Product NDC 51655-240
Product ID 51655-240_48d2d970-b305-2ef9-e063-6394a90a324a
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA070184
Listing Expiration 2027-12-31
Marketing Start 2022-10-06

Pharmacologic Class

Classes
dopamine d2 antagonists [moa] dopamine-2 receptor antagonist [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 51655240
Hyphenated Format 51655-240

Supplemental Identifiers

RxCUI
311666
UNII
W1792A2RVD

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name metoclopramide (source: ndc)
Generic Name metoclopramide (source: ndc)
Application Number ANDA070184 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE, PLASTIC (51655-240-52)
  • 6 TABLET in 1 BOTTLE, PLASTIC (51655-240-87)
source: ndc

Packages (2)

Ingredients (1)

metoclopramide hydrochloride (10 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "48d2d970-b305-2ef9-e063-6394a90a324a", "openfda": {"unii": ["W1792A2RVD"], "rxcui": ["311666"], "spl_set_id": ["f2b732ab-b859-7252-e053-2995a90af0d8"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (51655-240-52)", "package_ndc": "51655-240-52", "marketing_start_date": "20221006"}, {"sample": false, "description": "6 TABLET in 1 BOTTLE, PLASTIC (51655-240-87)", "package_ndc": "51655-240-87", "marketing_start_date": "20231226"}], "brand_name": "Metoclopramide", "product_id": "51655-240_48d2d970-b305-2ef9-e063-6394a90a324a", "dosage_form": "TABLET", "pharm_class": ["Dopamine D2 Antagonists [MoA]", "Dopamine-2 Receptor Antagonist [EPC]"], "product_ndc": "51655-240", "generic_name": "Metoclopramide", "labeler_name": "Northwind Health Company, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Metoclopramide", "active_ingredients": [{"name": "METOCLOPRAMIDE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA070184", "marketing_category": "ANDA", "marketing_start_date": "20221006", "listing_expiration_date": "20271231"}