metoclopramide

Generic: metoclopramide

Labeler: mylan institutional inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name metoclopramide
Generic Name metoclopramide
Labeler mylan institutional inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

metoclopramide hydrochloride 10 mg/1

Manufacturer
Mylan Institutional Inc.

Identifiers & Regulatory

Product NDC 51079-888
Product ID 51079-888_3a866de8-d779-26e4-e063-6294a90abf6b
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA070184
Listing Expiration 2026-12-31
Marketing Start 2014-01-02

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 51079888
Hyphenated Format 51079-888

Supplemental Identifiers

RxCUI
311666 311668
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
  • 100 BLISTER PACK in 1 CARTON (51079-888-20) / 1 TABLET in 1 BLISTER PACK (51079-888-01)
source: ndc

Packages (1)

51079-888-20 100 BLISTER PACK in 1 CARTON (51079-888-20) / 1 TABLET in 1 BLISTER PACK (51079-888-01)

Ingredients (1)

metoclopramide hydrochloride (10 mg/1)

Linked Drug Pages (1)

Metoclopramide ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "3a866de8-d779-26e4-e063-6294a90abf6b", "openfda": {"unii": ["W1792A2RVD"], "rxcui": ["311666", "311668"], "spl_set_id": ["447dbb34-7903-4e6a-be31-48a0b0e0d2f5"], "manufacturer_name": ["Mylan Institutional Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 CARTON (51079-888-20)  / 1 TABLET in 1 BLISTER PACK (51079-888-01)", "package_ndc": "51079-888-20", "marketing_start_date": "20140102"}], "brand_name": "Metoclopramide", "product_id": "51079-888_3a866de8-d779-26e4-e063-6294a90abf6b", "dosage_form": "TABLET", "pharm_class": ["Dopamine D2 Antagonists [MoA]", "Dopamine-2 Receptor Antagonist [EPC]"], "product_ndc": "51079-888", "generic_name": "Metoclopramide", "labeler_name": "Mylan Institutional Inc.", "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": "20140102", "listing_expiration_date": "20261231"}