Package 66267-841-06

Brand: metoclopramide

Generic: metoclopramide
NDC Package

Package Facts

Identity

Package NDC 66267-841-06
Digits Only 6626784106
Product NDC 66267-841
Product ID 66267-841_1fa77075-a19b-971d-e063-6294a90a255d
Description

6 TABLET in 1 BOTTLE (66267-841-06)

Marketing

Marketing Status
Marketed Since 2017-01-24
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": "1fa77075-a19b-971d-e063-6294a90a255d", "openfda": {"upc": ["0366267841061"], "unii": ["W1792A2RVD"], "rxcui": ["311668"], "spl_set_id": ["46dcafbc-9d50-316a-e054-00144ff88e88"], "manufacturer_name": ["NuCare Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "6 TABLET in 1 BOTTLE (66267-841-06)", "package_ndc": "66267-841-06", "marketing_start_date": "20170124"}], "brand_name": "Metoclopramide", "product_id": "66267-841_1fa77075-a19b-971d-e063-6294a90a255d", "dosage_form": "TABLET", "pharm_class": ["Dopamine D2 Antagonists [MoA]", "Dopamine-2 Receptor Antagonist [EPC]"], "product_ndc": "66267-841", "generic_name": "Metoclopramide", "labeler_name": "NuCare Pharmaceuticals, 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": "19930701", "listing_expiration_date": "20261231"}