metoclopramide

Generic: metoclopramide

Labeler: ani pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG NDA AUTHORIZED GENERIC Inactive Finished

Drug Facts

Product Profile

Brand Name metoclopramide
Generic Name metoclopramide
Labeler ani pharmaceuticals, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

metoclopramide hydrochloride 10 mg/1

Manufacturer
ANI Pharmaceuticals, Inc.

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 62559296
Hyphenated Format 62559-296

Supplemental Identifiers

RxCUI
311666 311668
UPC
0362559296014 0362559295017
UNII
W1792A2RVD

Packaging Origin

Original Packager
true

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
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE, PLASTIC (62559-296-01)
source: ndc

Packages (1)

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": "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"}