metoclopramide
Generic: metoclopramide
Labeler: hospira, inc.Drug Facts
Product Profile
Brand Name
metoclopramide
Generic Name
metoclopramide
Labeler
hospira, inc.
Dosage Form
INJECTION, SOLUTION
Routes
Active Ingredients
metoclopramide hydrochloride 5 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
0409-3414
Product ID
0409-3414_393f05e1-f40a-4d7e-8bf7-89bcd4c09b6b
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA073118
Listing Expiration
2026-12-31
Marketing Start
2006-02-02
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
04093414
Hyphenated Format
0409-3414
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
ANDA073118 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 5 mg/mL
Packaging
- 25 VIAL, SINGLE-DOSE in 1 TRAY (0409-3414-01) / 2 mL in 1 VIAL, SINGLE-DOSE (0409-3414-18)
- 25 VIAL, SINGLE-DOSE in 1 TRAY (0409-3414-11) / 2 mL in 1 VIAL, SINGLE-DOSE (0409-3414-21)
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "393f05e1-f40a-4d7e-8bf7-89bcd4c09b6b", "openfda": {"unii": ["W1792A2RVD"], "rxcui": ["311670"], "spl_set_id": ["373ba08b-33ad-49fc-28a7-928e89a65314"], "manufacturer_name": ["Hospira, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL, SINGLE-DOSE in 1 TRAY (0409-3414-01) / 2 mL in 1 VIAL, SINGLE-DOSE (0409-3414-18)", "package_ndc": "0409-3414-01", "marketing_start_date": "20060202"}, {"sample": false, "description": "25 VIAL, SINGLE-DOSE in 1 TRAY (0409-3414-11) / 2 mL in 1 VIAL, SINGLE-DOSE (0409-3414-21)", "package_ndc": "0409-3414-11", "marketing_start_date": "20240826"}], "brand_name": "Metoclopramide", "product_id": "0409-3414_393f05e1-f40a-4d7e-8bf7-89bcd4c09b6b", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Dopamine D2 Antagonists [MoA]", "Dopamine-2 Receptor Antagonist [EPC]"], "product_ndc": "0409-3414", "generic_name": "metoclopramide", "labeler_name": "Hospira, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Metoclopramide", "active_ingredients": [{"name": "METOCLOPRAMIDE HYDROCHLORIDE", "strength": "5 mg/mL"}], "application_number": "ANDA073118", "marketing_category": "ANDA", "marketing_start_date": "20060202", "listing_expiration_date": "20261231"}