metoclopramide
Generic: metoclopramide
Labeler: teva parenteral medicines, inc.Drug Facts
Product Profile
Brand Name
metoclopramide
Generic Name
metoclopramide
Labeler
teva parenteral medicines, inc.
Dosage Form
INJECTION, SOLUTION
Routes
Active Ingredients
metoclopramide hydrochloride 5 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
0703-4502
Product ID
0703-4502_fcb6627f-acef-46a6-afac-8830e27b38f1
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA073135
Listing Expiration
2026-12-31
Marketing Start
2024-09-04
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
07034502
Hyphenated Format
0703-4502
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
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
source: ndc
Resolved Composition
Strengths
- 5 mg/mL
Packaging
- 10 VIAL, SINGLE-USE in 1 CARTON (0703-4502-93) / 2 mL in 1 VIAL, SINGLE-USE (0703-4502-91)
Packages (1)
Ingredients (1)
Linked Drug Pages (2)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "fcb6627f-acef-46a6-afac-8830e27b38f1", "openfda": {"unii": ["W1792A2RVD"], "rxcui": ["311670"], "spl_set_id": ["5645a752-8868-4b51-8b59-48bb4276d763"], "manufacturer_name": ["Teva Parenteral Medicines, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL, SINGLE-USE in 1 CARTON (0703-4502-93) / 2 mL in 1 VIAL, SINGLE-USE (0703-4502-91)", "package_ndc": "0703-4502-93", "marketing_start_date": "20240904"}], "brand_name": "Metoclopramide", "product_id": "0703-4502_fcb6627f-acef-46a6-afac-8830e27b38f1", "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": "20240904", "listing_expiration_date": "20261231"}