Package 51662-1670-1

Brand: metoclopramide

Generic: metoclopramide
NDC Package

Package Facts

Identity

Package NDC 51662-1670-1
Digits Only 5166216701
Product NDC 51662-1670
Product ID 51662-1670_4046830f-4b88-5e6e-e063-6394a90aeeb8
Description

2 mL in 1 VIAL, SINGLE-DOSE (51662-1670-1)

Marketing

Marketing Status
Marketed Since 2006-02-02
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": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "4046830f-4b88-5e6e-e063-6394a90aeeb8", "openfda": {"unii": ["W1792A2RVD"], "rxcui": ["311670"], "spl_set_id": ["4046830f-4b87-5e6e-e063-6394a90aeeb8"], "manufacturer_name": ["HF Acquisition Co LLC, DBA HealthFirst"]}, "finished": true, "packaging": [{"sample": false, "description": "2 mL in 1 VIAL, SINGLE-DOSE (51662-1670-1)", "package_ndc": "51662-1670-1", "marketing_start_date": "20060202"}], "brand_name": "METOCLOPRAMIDE", "product_id": "51662-1670_4046830f-4b88-5e6e-e063-6394a90aeeb8", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Dopamine D2 Antagonists [MoA]", "Dopamine-2 Receptor Antagonist [EPC]"], "product_ndc": "51662-1670", "generic_name": "METOCLOPRAMIDE", "labeler_name": "HF Acquisition Co LLC, DBA HealthFirst", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "METOCLOPRAMIDE", "active_ingredients": [{"name": "METOCLOPRAMIDE HYDROCHLORIDE", "strength": "5 mg/mL"}], "application_number": "ANDA073118", "marketing_category": "ANDA", "marketing_start_date": "20060202", "listing_expiration_date": "20261231"}