metoclopramide
Generic: metoclopramide
Labeler: hf acquisition co llc, dba healthfirstDrug Facts
Product Profile
Brand Name
metoclopramide
Generic Name
metoclopramide
Labeler
hf acquisition co llc, dba healthfirst
Dosage Form
INJECTION, SOLUTION
Routes
Active Ingredients
metoclopramide hydrochloride 10 mg/2mL
Manufacturer
Identifiers & Regulatory
Product NDC
51662-1367
Product ID
51662-1367_ef7bd5a0-02a8-7b66-e053-2995a90a8ffa
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA091392
Listing Expiration
2026-12-31
Marketing Start
2019-10-14
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
516621367
Hyphenated Format
51662-1367
Supplemental Identifiers
RxCUI
UNII
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
ANDA091392 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 10 mg/2mL
Packaging
- 1 SYRINGE, GLASS in 1 BLISTER PACK (51662-1367-1) / 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": "ef7bd5a0-02a8-7b66-e053-2995a90a8ffa", "openfda": {"unii": ["W1792A2RVD"], "rxcui": ["727619"], "spl_set_id": ["94e5acdf-f19c-749a-e053-2995a90ae451"], "manufacturer_name": ["HF Acquisition Co LLC, DBA HealthFirst"]}, "finished": true, "packaging": [{"sample": false, "description": "1 SYRINGE, GLASS in 1 BLISTER PACK (51662-1367-1) / 2 mL in 1 SYRINGE, GLASS", "package_ndc": "51662-1367-1", "marketing_start_date": "20191014"}], "brand_name": "METOCLOPRAMIDE", "product_id": "51662-1367_ef7bd5a0-02a8-7b66-e053-2995a90a8ffa", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Dopamine D2 Antagonists [MoA]", "Dopamine-2 Receptor Antagonist [EPC]"], "product_ndc": "51662-1367", "generic_name": "METOCLOPRAMIDE", "labeler_name": "HF Acquisition Co LLC, DBA HealthFirst", "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": "20191014", "listing_expiration_date": "20261231"}