Package 84549-414-11

Brand: metoclopramide

Generic: metoclopramide
NDC Package

Package Facts

Identity

Package NDC 84549-414-11
Digits Only 8454941411
Product NDC 84549-414
Description

2 mL in 1 VIAL, SINGLE-DOSE (84549-414-11)

Marketing

Marketing Status
Marketed Since 2025-09-18
Brand metoclopramide
Generic metoclopramide
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "3f2b17ea-c266-0cd4-e063-6294a90a9d88", "openfda": {"unii": ["W1792A2RVD"], "rxcui": ["311670"], "spl_set_id": ["3f2b17ea-c265-0cd4-e063-6294a90a9d88"], "manufacturer_name": ["ProPharma Distribution"]}, "finished": true, "packaging": [{"sample": false, "description": "2 mL in 1 VIAL, SINGLE-DOSE (84549-414-11)", "package_ndc": "84549-414-11", "marketing_start_date": "20250918"}], "brand_name": "Metoclopramide", "product_id": "84549-414_3f2b17ea-c266-0cd4-e063-6294a90a9d88", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Dopamine D2 Antagonists [MoA]", "Dopamine-2 Receptor Antagonist [EPC]"], "product_ndc": "84549-414", "generic_name": "metoclopramide", "labeler_name": "ProPharma Distribution", "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"}