Package 68071-3924-3

Brand: metoclopramide

Generic: metoclopramide
NDC Package

Package Facts

Identity

Package NDC 68071-3924-3
Digits Only 6807139243
Product NDC 68071-3924
Product ID 68071-3924_45251536-a1a6-b87d-e063-6294a90a76ed
Description

30 TABLET in 1 BOTTLE (68071-3924-3)

Marketing

Marketing Status
Marketed Since 2025-12-04
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": "45251536-a1a6-b87d-e063-6294a90a76ed", "openfda": {"upc": ["0368071392432"], "unii": ["W1792A2RVD"], "rxcui": ["311668"], "spl_set_id": ["45250bbc-d079-c362-e063-6294a90a56e0"], "manufacturer_name": ["NuCare Pharamceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (68071-3924-3)", "package_ndc": "68071-3924-3", "marketing_start_date": "20251204"}], "brand_name": "Metoclopramide", "product_id": "68071-3924_45251536-a1a6-b87d-e063-6294a90a76ed", "dosage_form": "TABLET", "pharm_class": ["Dopamine D2 Antagonists [MoA]", "Dopamine-2 Receptor Antagonist [EPC]"], "product_ndc": "68071-3924", "generic_name": "Metoclopramide", "labeler_name": "NuCare Pharamceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Metoclopramide", "active_ingredients": [{"name": "METOCLOPRAMIDE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA072215", "marketing_category": "ANDA", "marketing_start_date": "20250212", "listing_expiration_date": "20261231"}