Package 70518-4541-0

Brand: metoclopramide

Generic: metoclopramide
NDC Package

Package Facts

Identity

Package NDC 70518-4541-0
Digits Only 7051845410
Product NDC 70518-4541
Product ID 70518-4541_4717fcb4-b7c0-f308-e063-6394a90a536e
Description

40 TABLET in 1 BOTTLE, PLASTIC (70518-4541-0)

Marketing

Marketing Status
Marketed Since 2025-12-23
Brand metoclopramide
Generic metoclopramide
Sample Package No

Linked Drug Pages (0)

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Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "4717fcb4-b7c0-f308-e063-6394a90a536e", "openfda": {"unii": ["W1792A2RVD"], "rxcui": ["311666"], "spl_set_id": ["c4828095-94e0-4f71-901c-93837974c658"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "40 TABLET in 1 BOTTLE, PLASTIC (70518-4541-0)", "package_ndc": "70518-4541-0", "marketing_start_date": "20251223"}], "brand_name": "Metoclopramide", "product_id": "70518-4541_4717fcb4-b7c0-f308-e063-6394a90a536e", "dosage_form": "TABLET", "pharm_class": ["Dopamine D2 Antagonists [MoA]", "Dopamine-2 Receptor Antagonist [EPC]"], "product_ndc": "70518-4541", "generic_name": "Metoclopramide", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Metoclopramide", "active_ingredients": [{"name": "METOCLOPRAMIDE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "NDA017854", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20251223", "listing_expiration_date": "20261231"}