metoclopramide

Generic: metoclopramide

Labeler: nucare pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

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

metoclopramide hydrochloride 10 mg/1

Manufacturer
NuCare Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 66267-286
Product ID 66267-286_1fa6ba1c-3f80-2089-e063-6294a90a11c7
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA070184
Listing Expiration 2026-12-31
Marketing Start 1990-09-30

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 66267286
Hyphenated Format 66267-286

Supplemental Identifiers

RxCUI
311666
UPC
0366267286305
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
  • 20 TABLET in 1 BOTTLE (66267-286-20)
  • 30 TABLET in 1 BOTTLE (66267-286-30)
  • 60 TABLET in 1 BOTTLE (66267-286-60)
source: ndc

Packages (3)

66267-286-20 20 TABLET in 1 BOTTLE (66267-286-20) 66267-286-30 30 TABLET in 1 BOTTLE (66267-286-30) 66267-286-60 60 TABLET in 1 BOTTLE (66267-286-60)

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": "1fa6ba1c-3f80-2089-e063-6294a90a11c7", "openfda": {"upc": ["0366267286305"], "unii": ["W1792A2RVD"], "rxcui": ["311666"], "spl_set_id": ["40cf021d-5f2a-055c-e054-00144ff88e88"], "manufacturer_name": ["NuCare Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET in 1 BOTTLE (66267-286-20)", "package_ndc": "66267-286-20", "marketing_start_date": "20161108"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (66267-286-30)", "package_ndc": "66267-286-30", "marketing_start_date": "20161108"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (66267-286-60)", "package_ndc": "66267-286-60", "marketing_start_date": "20161108"}], "brand_name": "Metoclopramide", "product_id": "66267-286_1fa6ba1c-3f80-2089-e063-6294a90a11c7", "dosage_form": "TABLET", "pharm_class": ["Dopamine D2 Antagonists [MoA]", "Dopamine-2 Receptor Antagonist [EPC]"], "product_ndc": "66267-286", "generic_name": "Metoclopramide", "labeler_name": "NuCare Pharmaceuticals, 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": "19900930", "listing_expiration_date": "20261231"}