Package 64950-344-16

Brand: metoclopramide

Generic: metoclopramide hydrochloride
NDC Package

Package Facts

Identity

Package NDC 64950-344-16
Digits Only 6495034416
Product NDC 64950-344
Description

473 mL in 1 BOTTLE, PLASTIC (64950-344-16)

Marketing

Marketing Status
Marketed Since 2024-06-01
Brand metoclopramide
Generic metoclopramide hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "c3ef09b0-2ebe-43d3-abb3-35aaca75e1c8", "openfda": {"unii": ["W1792A2RVD"], "rxcui": ["104884"], "spl_set_id": ["74358569-7a24-4a59-a7fc-500d2341d6cb"], "manufacturer_name": ["Genus Lifesciences Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "473 mL in 1 BOTTLE, PLASTIC (64950-344-16)", "package_ndc": "64950-344-16", "marketing_start_date": "20240601"}], "brand_name": "Metoclopramide", "product_id": "64950-344_c3ef09b0-2ebe-43d3-abb3-35aaca75e1c8", "dosage_form": "SOLUTION", "pharm_class": ["Dopamine D2 Antagonists [MoA]", "Dopamine-2 Receptor Antagonist [EPC]"], "product_ndc": "64950-344", "generic_name": "Metoclopramide Hydrochloride", "labeler_name": "Genus Lifesciences Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Metoclopramide", "active_ingredients": [{"name": "METOCLOPRAMIDE HYDROCHLORIDE", "strength": "5 mg/5mL"}], "application_number": "ANDA072744", "marketing_category": "ANDA", "marketing_start_date": "20240601", "listing_expiration_date": "20261231"}