metoclopramide

Generic: metoclopramide

Labeler: ipca laboratories limited
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name metoclopramide
Generic Name metoclopramide
Labeler ipca laboratories limited
Dosage Form TABLET
Routes
ORAL
Active Ingredients

metoclopramide hydrochloride 10 mg/1

Manufacturer
Ipca Laboratories Limited

Identifiers & Regulatory

Product NDC 83980-011
Product ID 83980-011_045886c5-5926-4d9e-a13c-8b0efc188862
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA078807
Listing Expiration 2026-12-31
Marketing Start 2025-01-09

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 83980011
Hyphenated Format 83980-011

Supplemental Identifiers

RxCUI
311666 311668
UPC
0383980011014 0383980010017
UNII
W1792A2RVD

Packaging Origin

Original Packager
true

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 ANDA078807 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (83980-011-01)
  • 500 TABLET in 1 BOTTLE (83980-011-05)
  • 1000 TABLET in 1 BOTTLE (83980-011-10)
  • 30 TABLET in 1 BOTTLE (83980-011-13)
source: ndc

Packages (4)

83980-011-01 100 TABLET in 1 BOTTLE (83980-011-01) 83980-011-05 500 TABLET in 1 BOTTLE (83980-011-05) 83980-011-10 1000 TABLET in 1 BOTTLE (83980-011-10) 83980-011-13 30 TABLET in 1 BOTTLE (83980-011-13)

Ingredients (1)

metoclopramide hydrochloride (10 mg/1)

Linked Drug Pages (1)

Metoclopramide ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "045886c5-5926-4d9e-a13c-8b0efc188862", "openfda": {"upc": ["0383980011014", "0383980010017"], "unii": ["W1792A2RVD"], "rxcui": ["311666", "311668"], "spl_set_id": ["c143e210-4ce7-44e5-b1e2-bf0e6bfde485"], "manufacturer_name": ["Ipca Laboratories Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (83980-011-01)", "package_ndc": "83980-011-01", "marketing_start_date": "20250109"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (83980-011-05)", "package_ndc": "83980-011-05", "marketing_start_date": "20250109"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (83980-011-10)", "package_ndc": "83980-011-10", "marketing_start_date": "20250109"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (83980-011-13)", "package_ndc": "83980-011-13", "marketing_start_date": "20250109"}], "brand_name": "Metoclopramide", "product_id": "83980-011_045886c5-5926-4d9e-a13c-8b0efc188862", "dosage_form": "TABLET", "pharm_class": ["Dopamine D2 Antagonists [MoA]", "Dopamine-2 Receptor Antagonist [EPC]"], "product_ndc": "83980-011", "generic_name": "Metoclopramide", "labeler_name": "Ipca Laboratories Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Metoclopramide", "active_ingredients": [{"name": "METOCLOPRAMIDE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA078807", "marketing_category": "ANDA", "marketing_start_date": "20250109", "listing_expiration_date": "20261231"}