metoclopramide

Generic: metoclopramide

Labeler: remedyrepack inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name metoclopramide
Generic Name metoclopramide
Labeler remedyrepack inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

metoclopramide hydrochloride 10 mg/1

Manufacturer
REMEDYREPACK INC.

Identifiers & Regulatory

Product NDC 70518-0669
Product ID 70518-0669_47fb319a-81e5-54ea-e063-6394a90ad250
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA070184
Listing Expiration 2027-12-31
Marketing Start 2019-08-14

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 705180669
Hyphenated Format 70518-0669

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 BLISTER PACK (70518-0669-0)
source: ndc

Packages (1)

70518-0669-0 30 TABLET in 1 BLISTER PACK (70518-0669-0)

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": "47fb319a-81e5-54ea-e063-6394a90ad250", "openfda": {"unii": ["W1792A2RVD"], "rxcui": ["311666"], "spl_set_id": ["6637cb78-d50a-4dbf-8fb7-b1b5102c5c5f"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (70518-0669-0)", "package_ndc": "70518-0669-0", "marketing_start_date": "20190814"}], "brand_name": "Metoclopramide", "product_id": "70518-0669_47fb319a-81e5-54ea-e063-6394a90ad250", "dosage_form": "TABLET", "pharm_class": ["Dopamine D2 Antagonists [MoA]", "Dopamine-2 Receptor Antagonist [EPC]"], "product_ndc": "70518-0669", "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": "20190814", "listing_expiration_date": "20271231"}