Package 42291-596-90

Brand: metoclopramide

Generic: metoclopramide
NDC Package

Package Facts

Identity

Package NDC 42291-596-90
Digits Only 4229159690
Product NDC 42291-596
Product ID 42291-596_4870ff00-f729-814d-e063-6394a90a6c8e
Description

90 TABLET in 1 BOTTLE (42291-596-90)

Marketing

Marketing Status
Marketed Since 2014-10-01
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": "4870ff00-f729-814d-e063-6394a90a6c8e", "openfda": {"upc": ["0342291595903", "0342291596900"], "unii": ["W1792A2RVD"], "rxcui": ["311666", "311668"], "spl_set_id": ["ff067ac5-6efc-3e86-e6d5-590b2779491c"], "manufacturer_name": ["AvKARE"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (42291-596-90)", "package_ndc": "42291-596-90", "marketing_start_date": "20141001"}], "brand_name": "Metoclopramide", "product_id": "42291-596_4870ff00-f729-814d-e063-6394a90a6c8e", "dosage_form": "TABLET", "pharm_class": ["Dopamine D2 Antagonists [MoA]", "Dopamine-2 Receptor Antagonist [EPC]"], "product_ndc": "42291-596", "generic_name": "Metoclopramide", "labeler_name": "AvKARE", "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": "20141001", "listing_expiration_date": "20271231"}