Package 0703-4502-04
Brand: metoclopramide
Generic: metoclopramidePackage Facts
Identity
Package NDC
0703-4502-04
Digits Only
0703450204
Product NDC
0703-4502
Description
25 VIAL, SINGLE-USE in 1 TRAY (0703-4502-04) / 2 mL in 1 VIAL, SINGLE-USE (0703-4502-01)
Marketing
Marketing Status
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": "e640a87c-7ee3-4ca2-9808-3916bfd1a54b", "openfda": {"unii": ["W1792A2RVD"], "rxcui": ["311670"], "spl_set_id": ["cccf04bd-7463-40b8-a41f-cb1093c358d7"], "manufacturer_name": ["Teva Parenteral Medicines, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL, SINGLE-USE in 1 TRAY (0703-4502-04) / 2 mL in 1 VIAL, SINGLE-USE (0703-4502-01)", "package_ndc": "0703-4502-04", "marketing_start_date": "19911201"}], "brand_name": "Metoclopramide", "product_id": "0703-4502_e640a87c-7ee3-4ca2-9808-3916bfd1a54b", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Dopamine D2 Antagonists [MoA]", "Dopamine-2 Receptor Antagonist [EPC]"], "product_ndc": "0703-4502", "generic_name": "Metoclopramide", "labeler_name": "Teva Parenteral Medicines, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Metoclopramide", "active_ingredients": [{"name": "METOCLOPRAMIDE HYDROCHLORIDE", "strength": "5 mg/mL"}], "application_number": "ANDA073135", "marketing_category": "ANDA", "marketing_start_date": "19911201", "listing_expiration_date": "20261231"}