metoclopramide

Generic: metoclopramide

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

Drug Facts

Product Profile

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

metoclopramide hydrochloride 10 mg/1

Manufacturer
ScieGen Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 50228-233
Product ID 50228-233_348f148b-3e1a-fe2d-e063-6294a90a9b22
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA072215
Listing Expiration 2026-12-31
Marketing Start 2025-02-12

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 50228233
Hyphenated Format 50228-233

Supplemental Identifiers

RxCUI
311666 311668
UPC
0350228232050 0350228233057
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 ANDA072215 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (50228-233-01)
  • 500 TABLET in 1 BOTTLE (50228-233-05)
  • 1000 TABLET in 1 BOTTLE (50228-233-10)
source: ndc

Packages (3)

50228-233-01 100 TABLET in 1 BOTTLE (50228-233-01) 50228-233-05 500 TABLET in 1 BOTTLE (50228-233-05) 50228-233-10 1000 TABLET in 1 BOTTLE (50228-233-10)

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": "348f148b-3e1a-fe2d-e063-6294a90a9b22", "openfda": {"upc": ["0350228232050", "0350228233057"], "unii": ["W1792A2RVD"], "rxcui": ["311666", "311668"], "spl_set_id": ["b16ad17c-eeea-407e-91e4-36506e9aa698"], "manufacturer_name": ["ScieGen Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (50228-233-01)", "package_ndc": "50228-233-01", "marketing_start_date": "20250212"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (50228-233-05)", "package_ndc": "50228-233-05", "marketing_start_date": "20250212"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (50228-233-10)", "package_ndc": "50228-233-10", "marketing_start_date": "20250212"}], "brand_name": "Metoclopramide", "product_id": "50228-233_348f148b-3e1a-fe2d-e063-6294a90a9b22", "dosage_form": "TABLET", "pharm_class": ["Dopamine D2 Antagonists [MoA]", "Dopamine-2 Receptor Antagonist [EPC]"], "product_ndc": "50228-233", "generic_name": "Metoclopramide", "labeler_name": "ScieGen Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Metoclopramide", "active_ingredients": [{"name": "METOCLOPRAMIDE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA072215", "marketing_category": "ANDA", "marketing_start_date": "20250212", "listing_expiration_date": "20261231"}