metoclopramide
Generic: metoclopramide
Labeler: remedyrepack inc.Drug Facts
Product Profile
Brand Name
metoclopramide
Generic Name
metoclopramide
Labeler
remedyrepack inc.
Dosage Form
TABLET
Routes
Active Ingredients
metoclopramide hydrochloride 10 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
70518-1193
Product ID
70518-1193_48c087f3-b411-b79b-e063-6294a90afce3
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA070184
Listing Expiration
2027-12-31
Marketing Start
2018-05-14
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
705181193
Hyphenated Format
70518-1193
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
ANDA070184 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 10 mg/1
Packaging
- 60 TABLET in 1 BOTTLE, PLASTIC (70518-1193-0)
- 10 TABLET in 1 BOTTLE, PLASTIC (70518-1193-4)
- 40 TABLET in 1 BOTTLE, PLASTIC (70518-1193-5)
Packages (3)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "48c087f3-b411-b79b-e063-6294a90afce3", "openfda": {"unii": ["W1792A2RVD"], "rxcui": ["311666"], "spl_set_id": ["5d31d815-50fa-4e78-8ebd-affc2514ce78"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET in 1 BOTTLE, PLASTIC (70518-1193-0)", "package_ndc": "70518-1193-0", "marketing_start_date": "20180514"}, {"sample": false, "description": "10 TABLET in 1 BOTTLE, PLASTIC (70518-1193-4)", "package_ndc": "70518-1193-4", "marketing_start_date": "20241125"}, {"sample": false, "description": "40 TABLET in 1 BOTTLE, PLASTIC (70518-1193-5)", "package_ndc": "70518-1193-5", "marketing_start_date": "20251118"}], "brand_name": "Metoclopramide", "product_id": "70518-1193_48c087f3-b411-b79b-e063-6294a90afce3", "dosage_form": "TABLET", "pharm_class": ["Dopamine D2 Antagonists [MoA]", "Dopamine-2 Receptor Antagonist [EPC]"], "product_ndc": "70518-1193", "generic_name": "Metoclopramide", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Metoclopramide", "active_ingredients": [{"name": "METOCLOPRAMIDE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA070184", "marketing_category": "ANDA", "marketing_start_date": "20180514", "listing_expiration_date": "20271231"}