Package 70518-0669-0

Brand: metoclopramide

Generic: metoclopramide
NDC Package

Package Facts

Identity

Package NDC 70518-0669-0
Digits Only 7051806690
Product NDC 70518-0669
Product ID 70518-0669_47fb319a-81e5-54ea-e063-6394a90ad250
Description

30 TABLET in 1 BLISTER PACK (70518-0669-0)

Marketing

Marketing Status
Marketed Since 2019-08-14
Brand metoclopramide
Generic metoclopramide
Sample Package No

Linked Drug Pages (1)

Metoclopramide ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "47fb319a-81e5-54ea-e063-6394a90ad250", "openfda": {"unii": ["W1792A2RVD"], "rxcui": ["311666"], "spl_set_id": ["6637cb78-d50a-4dbf-8fb7-b1b5102c5c5f"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (70518-0669-0)", "package_ndc": "70518-0669-0", "marketing_start_date": "20190814"}], "brand_name": "Metoclopramide", "product_id": "70518-0669_47fb319a-81e5-54ea-e063-6394a90ad250", "dosage_form": "TABLET", "pharm_class": ["Dopamine D2 Antagonists [MoA]", "Dopamine-2 Receptor Antagonist [EPC]"], "product_ndc": "70518-0669", "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": "ANDA070184", "marketing_category": "ANDA", "marketing_start_date": "20190814", "listing_expiration_date": "20271231"}