metoclopramide
Generic: metoclopramide
Labeler: northwind health company, llcDrug Facts
Product Profile
Brand Name
metoclopramide
Generic Name
metoclopramide
Labeler
northwind health company, llc
Dosage Form
TABLET
Routes
Active Ingredients
metoclopramide hydrochloride 10 mg/1
Manufacturer
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
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
51655240
Hyphenated Format
51655-240
Supplemental Identifiers
RxCUI
UNII
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
source: ndc
Resolved Composition
Strengths
- 10 mg/1
Packaging
- 30 TABLET in 1 BOTTLE, PLASTIC (51655-240-52)
- 6 TABLET in 1 BOTTLE, PLASTIC (51655-240-87)
Packages (2)
Ingredients (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"}