Package 51655-240-52

Brand: metoclopramide

Generic: metoclopramide
NDC Package

Package Facts

Identity

Package NDC 51655-240-52
Digits Only 5165524052
Product NDC 51655-240
Description

30 TABLET in 1 BOTTLE, PLASTIC (51655-240-52)

Marketing

Marketing Status
Marketed Since 2022-10-06
Brand metoclopramide
Generic metoclopramide
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "48d2d970-b305-2ef9-e063-6394a90a324a", "openfda": {"unii": ["W1792A2RVD"], "rxcui": ["311666"], "spl_set_id": ["f2b732ab-b859-7252-e053-2995a90af0d8"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (51655-240-52)", "package_ndc": "51655-240-52", "marketing_start_date": "20221006"}, {"sample": false, "description": "6 TABLET in 1 BOTTLE, PLASTIC (51655-240-87)", "package_ndc": "51655-240-87", "marketing_start_date": "20231226"}], "brand_name": "Metoclopramide", "product_id": "51655-240_48d2d970-b305-2ef9-e063-6394a90a324a", "dosage_form": "TABLET", "pharm_class": ["Dopamine D2 Antagonists [MoA]", "Dopamine-2 Receptor Antagonist [EPC]"], "product_ndc": "51655-240", "generic_name": "Metoclopramide", "labeler_name": "Northwind Health Company, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Metoclopramide", "active_ingredients": [{"name": "METOCLOPRAMIDE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA070184", "marketing_category": "ANDA", "marketing_start_date": "20221006", "listing_expiration_date": "20271231"}