metoclopramide

Generic: metoclopramide

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

Drug Facts

Product Profile

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

metoclopramide hydrochloride 5 mg/1

Manufacturer
Teva Pharmaceuticals USA, Inc.

Identifiers & Regulatory

Product NDC 0093-2204
Product ID 0093-2204_8f208d35-b19b-40a1-b363-f44ff08ec3d6
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA072801
Listing Expiration 2026-12-31
Marketing Start 1993-07-01

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 00932204
Hyphenated Format 0093-2204

Supplemental Identifiers

RxCUI
311666 311668
UPC
0300932204010 0300932203013
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 ANDA072801 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 5 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (0093-2204-01)
  • 500 TABLET in 1 BOTTLE (0093-2204-05)
source: ndc

Packages (2)

0093-2204-01 100 TABLET in 1 BOTTLE (0093-2204-01) 0093-2204-05 500 TABLET in 1 BOTTLE (0093-2204-05)

Ingredients (1)

metoclopramide hydrochloride (5 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": "8f208d35-b19b-40a1-b363-f44ff08ec3d6", "openfda": {"upc": ["0300932204010", "0300932203013"], "unii": ["W1792A2RVD"], "rxcui": ["311666", "311668"], "spl_set_id": ["e15905e0-e0f6-4c8b-ac19-59724d6c4bf0"], "manufacturer_name": ["Teva Pharmaceuticals USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (0093-2204-01)", "package_ndc": "0093-2204-01", "marketing_start_date": "19930701"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (0093-2204-05)", "package_ndc": "0093-2204-05", "marketing_start_date": "19930701"}], "brand_name": "Metoclopramide", "product_id": "0093-2204_8f208d35-b19b-40a1-b363-f44ff08ec3d6", "dosage_form": "TABLET", "pharm_class": ["Dopamine D2 Antagonists [MoA]", "Dopamine-2 Receptor Antagonist [EPC]"], "product_ndc": "0093-2204", "generic_name": "Metoclopramide", "labeler_name": "Teva Pharmaceuticals USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Metoclopramide", "active_ingredients": [{"name": "METOCLOPRAMIDE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA072801", "marketing_category": "ANDA", "marketing_start_date": "19930701", "listing_expiration_date": "20261231"}