metoclopramide
Generic: metoclopramide
Labeler: redpharm drugDrug Facts
Product Profile
Brand Name
metoclopramide
Generic Name
metoclopramide
Labeler
redpharm drug
Dosage Form
TABLET
Routes
Active Ingredients
metoclopramide hydrochloride 5 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
67296-2213
Product ID
67296-2213_49eb7254-b7f9-6119-e063-6394a90aaf3d
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
NDA AUTHORIZED GENERIC
Application Number
NDA017854
Listing Expiration
2027-12-31
Marketing Start
2021-12-13
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
672962213
Hyphenated Format
67296-2213
Supplemental Identifiers
RxCUI
UPC
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
NDA017854 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 5 mg/1
Packaging
- 15 TABLET in 1 BOTTLE, PLASTIC (67296-2213-1)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "49eb7254-b7f9-6119-e063-6394a90aaf3d", "openfda": {"upc": ["0362559296014", "0362559295017"], "unii": ["W1792A2RVD"], "rxcui": ["311668"], "spl_set_id": ["49eb807b-fa34-3d84-e063-6394a90acfcf"], "manufacturer_name": ["Redpharm Drug"]}, "finished": true, "packaging": [{"sample": false, "description": "15 TABLET in 1 BOTTLE, PLASTIC (67296-2213-1)", "package_ndc": "67296-2213-1", "marketing_start_date": "20211213"}], "brand_name": "Metoclopramide", "product_id": "67296-2213_49eb7254-b7f9-6119-e063-6394a90aaf3d", "dosage_form": "TABLET", "pharm_class": ["Dopamine D2 Antagonists [MoA]", "Dopamine-2 Receptor Antagonist [EPC]"], "product_ndc": "67296-2213", "generic_name": "Metoclopramide", "labeler_name": "Redpharm Drug", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Metoclopramide", "active_ingredients": [{"name": "METOCLOPRAMIDE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "NDA017854", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20211213", "listing_expiration_date": "20271231"}