metoclopramide hydrochloride
Generic: metoclopramide hydrochloride
Labeler: lupin pharmaceuticals,inc.Drug Facts
Product Profile
Brand Name
metoclopramide hydrochloride
Generic Name
metoclopramide hydrochloride
Labeler
lupin pharmaceuticals,inc.
Dosage Form
TABLET, ORALLY DISINTEGRATING
Routes
Active Ingredients
metoclopramide hydrochloride 10 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
43386-580
Product ID
43386-580_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
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
43386580
Hyphenated Format
43386-580
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
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
source: ndc
Resolved Composition
Strengths
- 10 mg/1
Packaging
- 1 BLISTER PACK in 1 CARTON (43386-580-31) / 10 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK
Packages (1)
Ingredients (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 (43386-580-31) / 10 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK", "package_ndc": "43386-580-31", "marketing_start_date": "20150406"}], "brand_name": "METOCLOPRAMIDE hydrochloride", "product_id": "43386-580_b5844be2-94b3-3e3f-e053-2995a90a6eb8", "dosage_form": "TABLET, ORALLY DISINTEGRATING", "pharm_class": ["Dopamine D2 Antagonists [MoA]", "Dopamine-2 Receptor Antagonist [EPC]"], "product_ndc": "43386-580", "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": "10 mg/1"}], "application_number": "ANDA202191", "marketing_category": "ANDA", "marketing_start_date": "20150406", "listing_expiration_date": "20261231"}