metoclopramide

Generic: metoclopramide

Labeler: teva parenteral medicines, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name metoclopramide
Generic Name metoclopramide
Labeler teva parenteral medicines, inc.
Dosage Form INJECTION, SOLUTION
Routes
INTRAMUSCULAR INTRAVENOUS
Active Ingredients

metoclopramide hydrochloride 5 mg/mL

Manufacturer
Teva Parenteral Medicines, Inc.

Identifiers & Regulatory

Product NDC 0703-4502
Product ID 0703-4502_e640a87c-7ee3-4ca2-9808-3916bfd1a54b
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA073135
Listing Expiration 2026-12-31
Marketing Start 1991-12-01

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 07034502
Hyphenated Format 0703-4502

Supplemental Identifiers

RxCUI
311670
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 ANDA073135 (source: ndc)
Routes
INTRAMUSCULAR INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 5 mg/mL
source: ndc
Packaging
  • 25 VIAL, SINGLE-USE in 1 TRAY (0703-4502-04) / 2 mL in 1 VIAL, SINGLE-USE (0703-4502-01)
source: ndc

Packages (1)

0703-4502-04 25 VIAL, SINGLE-USE in 1 TRAY (0703-4502-04) / 2 mL in 1 VIAL, SINGLE-USE (0703-4502-01)

Ingredients (1)

metoclopramide hydrochloride (5 mg/mL)

Linked Drug Pages (2)

Metoclopramide ndc-match (0.9) Metoclopramide ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "e640a87c-7ee3-4ca2-9808-3916bfd1a54b", "openfda": {"unii": ["W1792A2RVD"], "rxcui": ["311670"], "spl_set_id": ["cccf04bd-7463-40b8-a41f-cb1093c358d7"], "manufacturer_name": ["Teva Parenteral Medicines, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL, SINGLE-USE in 1 TRAY (0703-4502-04)  / 2 mL in 1 VIAL, SINGLE-USE (0703-4502-01)", "package_ndc": "0703-4502-04", "marketing_start_date": "19911201"}], "brand_name": "Metoclopramide", "product_id": "0703-4502_e640a87c-7ee3-4ca2-9808-3916bfd1a54b", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Dopamine D2 Antagonists [MoA]", "Dopamine-2 Receptor Antagonist [EPC]"], "product_ndc": "0703-4502", "generic_name": "Metoclopramide", "labeler_name": "Teva Parenteral Medicines, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Metoclopramide", "active_ingredients": [{"name": "METOCLOPRAMIDE HYDROCHLORIDE", "strength": "5 mg/mL"}], "application_number": "ANDA073135", "marketing_category": "ANDA", "marketing_start_date": "19911201", "listing_expiration_date": "20261231"}