Package 51079-886-20

Brand: metoclopramide

Generic: metoclopramide
NDC Package

Package Facts

Identity

Package NDC 51079-886-20
Digits Only 5107988620
Product NDC 51079-886
Product ID 51079-886_3a866de8-d779-26e4-e063-6294a90abf6b
Description

100 BLISTER PACK in 1 CARTON (51079-886-20) / 1 TABLET in 1 BLISTER PACK (51079-886-01)

Marketing

Marketing Status
Marketed Since 2013-12-30
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": "3a866de8-d779-26e4-e063-6294a90abf6b", "openfda": {"unii": ["W1792A2RVD"], "rxcui": ["311666", "311668"], "spl_set_id": ["447dbb34-7903-4e6a-be31-48a0b0e0d2f5"], "manufacturer_name": ["Mylan Institutional Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 CARTON (51079-886-20)  / 1 TABLET in 1 BLISTER PACK (51079-886-01)", "package_ndc": "51079-886-20", "marketing_start_date": "20131230"}], "brand_name": "Metoclopramide", "product_id": "51079-886_3a866de8-d779-26e4-e063-6294a90abf6b", "dosage_form": "TABLET", "pharm_class": ["Dopamine D2 Antagonists [MoA]", "Dopamine-2 Receptor Antagonist [EPC]"], "product_ndc": "51079-886", "generic_name": "Metoclopramide", "labeler_name": "Mylan Institutional Inc.", "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": "20131230", "listing_expiration_date": "20261231"}