metoclopramide
Generic: metoclopramide
Labeler: ani pharmaceuticals, inc.Drug Facts
Product Profile
Brand Name
metoclopramide
Generic Name
metoclopramide
Labeler
ani pharmaceuticals, inc.
Dosage Form
TABLET
Routes
Active Ingredients
metoclopramide hydrochloride 10 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
62559-296
Product ID
62559-296_64aa5644-d882-4850-8fc2-eddc7dd12307
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
NDA AUTHORIZED GENERIC
Application Number
NDA017854
Listing Expiration
2026-12-31
Marketing Start
2021-12-13
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
62559296
Hyphenated Format
62559-296
Supplemental Identifiers
RxCUI
UPC
UNII
Packaging Origin
Original Packager
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
NDA017854 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 10 mg/1
Packaging
- 100 TABLET in 1 BOTTLE, PLASTIC (62559-296-01)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "64aa5644-d882-4850-8fc2-eddc7dd12307", "openfda": {"upc": ["0362559296014", "0362559295017"], "unii": ["W1792A2RVD"], "rxcui": ["311666", "311668"], "spl_set_id": ["797aad80-0597-42f8-99d5-39de180c3b5a"], "manufacturer_name": ["ANI Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (62559-296-01)", "package_ndc": "62559-296-01", "marketing_start_date": "20211213"}], "brand_name": "Metoclopramide", "product_id": "62559-296_64aa5644-d882-4850-8fc2-eddc7dd12307", "dosage_form": "TABLET", "pharm_class": ["Dopamine D2 Antagonists [MoA]", "Dopamine-2 Receptor Antagonist [EPC]"], "product_ndc": "62559-296", "generic_name": "Metoclopramide", "labeler_name": "ANI Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Metoclopramide", "active_ingredients": [{"name": "METOCLOPRAMIDE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "NDA017854", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20211213", "listing_expiration_date": "20261231"}