metoclopramide hydrochloride

Generic: metoclopramide hydrochloride

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

Drug Facts

Product Profile

Brand Name metoclopramide hydrochloride
Generic Name metoclopramide hydrochloride
Labeler lupin pharmaceuticals,inc.
Dosage Form TABLET, ORALLY DISINTEGRATING
Routes
ORAL
Active Ingredients

metoclopramide hydrochloride 5 mg/1

Manufacturer
Lupin Pharmaceuticals,Inc.

Identifiers & Regulatory

Product NDC 43386-581
Product ID 43386-581_b5844be2-94b3-3e3f-e053-2995a90a6eb8
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA202191
Listing Expiration 2026-12-31
Marketing Start 2015-04-06

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 43386581
Hyphenated Format 43386-581

Supplemental Identifiers

RxCUI
608623 608624
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 hydrochloride (source: ndc)
Generic Name metoclopramide hydrochloride (source: ndc)
Application Number ANDA202191 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 5 mg/1
source: ndc
Packaging
  • 1 BLISTER PACK in 1 CARTON (43386-581-31) / 10 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK
source: ndc

Packages (1)

Ingredients (1)

metoclopramide hydrochloride (5 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "b5844be2-94b3-3e3f-e053-2995a90a6eb8", "openfda": {"unii": ["W1792A2RVD"], "rxcui": ["608623", "608624"], "spl_set_id": ["7cd1dc35-2fb2-4f1d-8769-24c3c3aa34fa"], "manufacturer_name": ["Lupin Pharmaceuticals,Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BLISTER PACK in 1 CARTON (43386-581-31)  / 10 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK", "package_ndc": "43386-581-31", "marketing_start_date": "20150406"}], "brand_name": "METOCLOPRAMIDE hydrochloride", "product_id": "43386-581_b5844be2-94b3-3e3f-e053-2995a90a6eb8", "dosage_form": "TABLET, ORALLY DISINTEGRATING", "pharm_class": ["Dopamine D2 Antagonists [MoA]", "Dopamine-2 Receptor Antagonist [EPC]"], "product_ndc": "43386-581", "generic_name": "Metoclopramide Hydrochloride", "labeler_name": "Lupin Pharmaceuticals,Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "METOCLOPRAMIDE hydrochloride", "active_ingredients": [{"name": "METOCLOPRAMIDE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA202191", "marketing_category": "ANDA", "marketing_start_date": "20150406", "listing_expiration_date": "20261231"}