Package 67296-2213-1

Brand: metoclopramide

Generic: metoclopramide
NDC Package

Package Facts

Identity

Package NDC 67296-2213-1
Digits Only 6729622131
Product NDC 67296-2213
Product ID 67296-2213_49eb7254-b7f9-6119-e063-6394a90aaf3d
Description

15 TABLET in 1 BOTTLE, PLASTIC (67296-2213-1)

Marketing

Marketing Status
Marketed Since 2021-12-13
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": "49eb7254-b7f9-6119-e063-6394a90aaf3d", "openfda": {"upc": ["0362559296014", "0362559295017"], "unii": ["W1792A2RVD"], "rxcui": ["311668"], "spl_set_id": ["49eb807b-fa34-3d84-e063-6394a90acfcf"], "manufacturer_name": ["Redpharm Drug"]}, "finished": true, "packaging": [{"sample": false, "description": "15 TABLET in 1 BOTTLE, PLASTIC (67296-2213-1)", "package_ndc": "67296-2213-1", "marketing_start_date": "20211213"}], "brand_name": "Metoclopramide", "product_id": "67296-2213_49eb7254-b7f9-6119-e063-6394a90aaf3d", "dosage_form": "TABLET", "pharm_class": ["Dopamine D2 Antagonists [MoA]", "Dopamine-2 Receptor Antagonist [EPC]"], "product_ndc": "67296-2213", "generic_name": "Metoclopramide", "labeler_name": "Redpharm Drug", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Metoclopramide", "active_ingredients": [{"name": "METOCLOPRAMIDE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "NDA017854", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20211213", "listing_expiration_date": "20271231"}