metoclopramide

Generic: metoclopramide

Labeler: avkare
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name metoclopramide
Generic Name metoclopramide
Labeler avkare
Dosage Form TABLET
Routes
ORAL
Active Ingredients

metoclopramide hydrochloride 10 mg/1

Manufacturer
AvKARE

Identifiers & Regulatory

Product NDC 42291-596
Product ID 42291-596_4870ff00-f729-814d-e063-6394a90a6c8e
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA070184
Listing Expiration 2027-12-31
Marketing Start 2014-10-01

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 42291596
Hyphenated Format 42291-596

Supplemental Identifiers

RxCUI
311666 311668
UPC
0342291595903 0342291596900
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
  • 90 TABLET in 1 BOTTLE (42291-596-90)
source: ndc

Packages (1)

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": "4870ff00-f729-814d-e063-6394a90a6c8e", "openfda": {"upc": ["0342291595903", "0342291596900"], "unii": ["W1792A2RVD"], "rxcui": ["311666", "311668"], "spl_set_id": ["ff067ac5-6efc-3e86-e6d5-590b2779491c"], "manufacturer_name": ["AvKARE"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (42291-596-90)", "package_ndc": "42291-596-90", "marketing_start_date": "20141001"}], "brand_name": "Metoclopramide", "product_id": "42291-596_4870ff00-f729-814d-e063-6394a90a6c8e", "dosage_form": "TABLET", "pharm_class": ["Dopamine D2 Antagonists [MoA]", "Dopamine-2 Receptor Antagonist [EPC]"], "product_ndc": "42291-596", "generic_name": "Metoclopramide", "labeler_name": "AvKARE", "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": "20141001", "listing_expiration_date": "20271231"}