metoclopramide

Generic: metoclopramide

Labeler: nucare pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name metoclopramide
Generic Name metoclopramide
Labeler nucare pharmaceuticals, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

metoclopramide hydrochloride 5 mg/1

Manufacturer
NuCare Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 68071-3923
Product ID 68071-3923_4524065f-cc18-eeaa-e063-6394a90a3566
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA072801
Listing Expiration 2026-12-31
Marketing Start 1993-07-01

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 680713923
Hyphenated Format 68071-3923

Supplemental Identifiers

RxCUI
311668
UPC
0368071392333
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 ANDA072801 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 5 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (68071-3923-3)
source: ndc

Packages (1)

68071-3923-3 30 TABLET in 1 BOTTLE (68071-3923-3)

Ingredients (1)

metoclopramide hydrochloride (5 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": "4524065f-cc18-eeaa-e063-6394a90a3566", "openfda": {"upc": ["0368071392333"], "unii": ["W1792A2RVD"], "rxcui": ["311668"], "spl_set_id": ["4524146c-f588-083b-e063-6294a90ac977"], "manufacturer_name": ["NuCare Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (68071-3923-3)", "package_ndc": "68071-3923-3", "marketing_start_date": "20251204"}], "brand_name": "Metoclopramide", "product_id": "68071-3923_4524065f-cc18-eeaa-e063-6394a90a3566", "dosage_form": "TABLET", "pharm_class": ["Dopamine D2 Antagonists [MoA]", "Dopamine-2 Receptor Antagonist [EPC]"], "product_ndc": "68071-3923", "generic_name": "Metoclopramide", "labeler_name": "NuCare Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Metoclopramide", "active_ingredients": [{"name": "METOCLOPRAMIDE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA072801", "marketing_category": "ANDA", "marketing_start_date": "19930701", "listing_expiration_date": "20261231"}