Package 0615-7698-39

Brand: metoclopramide

Generic: metoclopramide
NDC Package

Package Facts

Identity

Package NDC 0615-7698-39
Digits Only 0615769839
Product NDC 0615-7698
Description

30 TABLET in 1 BLISTER PACK (0615-7698-39)

Marketing

Marketing Status
Marketed Since 2011-11-18
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": "c8471d07-1fca-4135-9b0e-cc9f5e037a18", "openfda": {"unii": ["W1792A2RVD"], "rxcui": ["311666", "311668"], "spl_set_id": ["4ab8ddab-8226-4b5a-8774-308ed49d6bc4"], "manufacturer_name": ["NCS HealthCare of KY, LLC dba Vangard Labs"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (0615-7698-39)", "package_ndc": "0615-7698-39", "marketing_start_date": "20111118"}], "brand_name": "Metoclopramide", "product_id": "0615-7698_c8471d07-1fca-4135-9b0e-cc9f5e037a18", "dosage_form": "TABLET", "pharm_class": ["Dopamine D2 Antagonists [MoA]", "Dopamine-2 Receptor Antagonist [EPC]"], "product_ndc": "0615-7698", "generic_name": "Metoclopramide", "labeler_name": "NCS HealthCare of KY, LLC dba Vangard Labs", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Metoclopramide", "active_ingredients": [{"name": "METOCLOPRAMIDE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA072801", "marketing_category": "ANDA", "marketing_start_date": "20111118", "listing_expiration_date": "20261231"}