metoclopramide
Generic: metoclopramide hydrochloride
Labeler: fresenius kabi usa, llcDrug Facts
Product Profile
Brand Name
metoclopramide
Generic Name
metoclopramide hydrochloride
Labeler
fresenius kabi usa, llc
Dosage Form
INJECTION, SOLUTION
Routes
Active Ingredients
metoclopramide hydrochloride 10 mg/2mL
Manufacturer
Identifiers & Regulatory
Product NDC
76045-213
Product ID
76045-213_4a411ded-d608-41d3-bb26-67d5d5d3c9b5
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA091392
Listing Expiration
2026-12-31
Marketing Start
2013-05-03
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
76045213
Hyphenated Format
76045-213
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 (source: ndc)
Generic Name
metoclopramide hydrochloride (source: ndc)
Application Number
ANDA091392 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 10 mg/2mL
Packaging
- 24 BLISTER PACK in 1 CARTON (76045-213-20) / 1 SYRINGE, GLASS in 1 BLISTER PACK (76045-213-00) / 2 mL in 1 SYRINGE, GLASS
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "4a411ded-d608-41d3-bb26-67d5d5d3c9b5", "openfda": {"unii": ["W1792A2RVD"], "rxcui": ["727619"], "spl_set_id": ["cc739885-e10e-4bcb-a781-c726c518f3d1"], "manufacturer_name": ["Fresenius Kabi USA, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "24 BLISTER PACK in 1 CARTON (76045-213-20) / 1 SYRINGE, GLASS in 1 BLISTER PACK (76045-213-00) / 2 mL in 1 SYRINGE, GLASS", "package_ndc": "76045-213-20", "marketing_start_date": "20220228"}], "brand_name": "Metoclopramide", "product_id": "76045-213_4a411ded-d608-41d3-bb26-67d5d5d3c9b5", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Dopamine D2 Antagonists [MoA]", "Dopamine-2 Receptor Antagonist [EPC]"], "product_ndc": "76045-213", "generic_name": "Metoclopramide Hydrochloride", "labeler_name": "Fresenius Kabi USA, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Metoclopramide", "active_ingredients": [{"name": "METOCLOPRAMIDE HYDROCHLORIDE", "strength": "10 mg/2mL"}], "application_number": "ANDA091392", "marketing_category": "ANDA", "marketing_start_date": "20130503", "listing_expiration_date": "20261231"}