metoclopramide
Generic: metoclopramide
Labeler: propharma distributionDrug Facts
Product Profile
Brand Name
metoclopramide
Generic Name
metoclopramide
Labeler
propharma distribution
Dosage Form
INJECTION, SOLUTION
Routes
Active Ingredients
metoclopramide hydrochloride 5 mg/mL
Manufacturer
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
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
84549414
Hyphenated Format
84549-414
Supplemental Identifiers
RxCUI
UNII
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
source: ndc
Resolved Composition
Strengths
- 5 mg/mL
Packaging
- 2 mL in 1 VIAL, SINGLE-DOSE (84549-414-11)
Packages (1)
Ingredients (1)
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"}