Package 68788-7930-3

Brand: metoclopramide

Generic: metoclopramide
NDC Package

Package Facts

Identity

Package NDC 68788-7930-3
Digits Only 6878879303
Product NDC 68788-7930
Product ID 68788-7930_47f3f4a8-595a-42f2-967f-958a7c8e9467
Description

30 TABLET in 1 BOTTLE (68788-7930-3)

Marketing

Marketing Status
Marketed Since 2021-06-15
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": "47f3f4a8-595a-42f2-967f-958a7c8e9467", "openfda": {"unii": ["W1792A2RVD"], "rxcui": ["311666"], "spl_set_id": ["697ec7b1-945a-4a31-b585-f051dc246165"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (68788-7930-3)", "package_ndc": "68788-7930-3", "marketing_start_date": "20210615"}], "brand_name": "Metoclopramide", "product_id": "68788-7930_47f3f4a8-595a-42f2-967f-958a7c8e9467", "dosage_form": "TABLET", "pharm_class": ["Dopamine D2 Antagonists [MoA]", "Dopamine-2 Receptor Antagonist [EPC]"], "product_ndc": "68788-7930", "generic_name": "Metoclopramide", "labeler_name": "Preferred Pharmaceuticals Inc.", "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": "20210615", "listing_expiration_date": "20261231"}