metoclopramide

Generic: metoclopramide

Labeler: propharma distribution
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name metoclopramide
Generic Name metoclopramide
Labeler propharma distribution
Dosage Form INJECTION, SOLUTION
Routes
INTRAMUSCULAR INTRAVENOUS
Active Ingredients

metoclopramide hydrochloride 5 mg/mL

Manufacturer
ProPharma Distribution

Identifiers & Regulatory

Product NDC 84549-414
Product ID 84549-414_3f2b17ea-c266-0cd4-e063-6294a90a9d88
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA073118
Listing Expiration 2026-12-31
Marketing Start 2006-02-02

Pharmacologic Class

Classes
dopamine d2 antagonists [moa] dopamine-2 receptor antagonist [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 84549414
Hyphenated Format 84549-414

Supplemental Identifiers

RxCUI
311670
UNII
W1792A2RVD

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name metoclopramide (source: ndc)
Generic Name metoclopramide (source: ndc)
Application Number ANDA073118 (source: ndc)
Routes
INTRAMUSCULAR INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 5 mg/mL
source: ndc
Packaging
  • 2 mL in 1 VIAL, SINGLE-DOSE (84549-414-11)
source: ndc

Packages (1)

Ingredients (1)

metoclopramide hydrochloride (5 mg/mL)

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"}