metoclopramide

Generic: metoclopramide

Labeler: bryant ranch prepack
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name metoclopramide
Generic Name metoclopramide
Labeler bryant ranch prepack
Dosage Form TABLET
Routes
ORAL
Active Ingredients

metoclopramide hydrochloride 10 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 71335-0362
Product ID 71335-0362_21012b46-95dc-4a07-8b81-c623eb771740
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA070184
Listing Expiration 2026-12-31
Marketing Start 1990-09-30

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 713350362
Hyphenated Format 71335-0362

Supplemental Identifiers

RxCUI
311666
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 ANDA070184 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (71335-0362-1)
  • 90 TABLET in 1 BOTTLE (71335-0362-2)
  • 60 TABLET in 1 BOTTLE (71335-0362-3)
  • 10 TABLET in 1 BOTTLE (71335-0362-4)
  • 20 TABLET in 1 BOTTLE (71335-0362-5)
  • 100 TABLET in 1 BOTTLE (71335-0362-6)
source: ndc

Packages (6)

Ingredients (1)

metoclopramide hydrochloride (10 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "21012b46-95dc-4a07-8b81-c623eb771740", "openfda": {"unii": ["W1792A2RVD"], "rxcui": ["311666"], "spl_set_id": ["23f11d3c-1529-4bb6-a61e-e4bab1a3e98e"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (71335-0362-1)", "package_ndc": "71335-0362-1", "marketing_start_date": "20180906"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (71335-0362-2)", "package_ndc": "71335-0362-2", "marketing_start_date": "20211229"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (71335-0362-3)", "package_ndc": "71335-0362-3", "marketing_start_date": "20211229"}, {"sample": false, "description": "10 TABLET in 1 BOTTLE (71335-0362-4)", "package_ndc": "71335-0362-4", "marketing_start_date": "20211229"}, {"sample": false, "description": "20 TABLET in 1 BOTTLE (71335-0362-5)", "package_ndc": "71335-0362-5", "marketing_start_date": "20211229"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (71335-0362-6)", "package_ndc": "71335-0362-6", "marketing_start_date": "20211229"}], "brand_name": "Metoclopramide", "product_id": "71335-0362_21012b46-95dc-4a07-8b81-c623eb771740", "dosage_form": "TABLET", "pharm_class": ["Dopamine D2 Antagonists [MoA]", "Dopamine-2 Receptor Antagonist [EPC]"], "product_ndc": "71335-0362", "generic_name": "Metoclopramide", "labeler_name": "Bryant Ranch Prepack", "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": "19900930", "listing_expiration_date": "20261231"}