metoclopramide
Generic: metoclopramide
Labeler: atlantic biologicals corp.Drug Facts
Product Profile
Brand Name
metoclopramide
Generic Name
metoclopramide
Labeler
atlantic biologicals corp.
Dosage Form
SOLUTION
Routes
Active Ingredients
metoclopramide hydrochloride 5 mg/5mL
Manufacturer
Identifiers & Regulatory
Product NDC
17856-1190
Product ID
17856-1190_3ce771f8-a078-c4ca-e063-6294a90ae2b2
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA071402
Listing Expiration
2026-12-31
Marketing Start
2015-05-18
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
178561190
Hyphenated Format
17856-1190
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
ANDA071402 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 5 mg/5mL
Packaging
- 72 CUP, UNIT-DOSE in 1 CASE (17856-1190-1) / 5 mL in 1 CUP, UNIT-DOSE
- 120 SYRINGE in 1 CASE (17856-1190-2) / 1 mL in 1 SYRINGE
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3ce771f8-a078-c4ca-e063-6294a90ae2b2", "openfda": {"unii": ["W1792A2RVD"], "rxcui": ["104884"], "spl_set_id": ["3ce3245f-7021-5135-e063-6394a90a7d95"], "manufacturer_name": ["ATLANTIC BIOLOGICALS CORP."]}, "finished": true, "packaging": [{"sample": false, "description": "72 CUP, UNIT-DOSE in 1 CASE (17856-1190-1) / 5 mL in 1 CUP, UNIT-DOSE", "package_ndc": "17856-1190-1", "marketing_start_date": "20250821"}, {"sample": false, "description": "120 SYRINGE in 1 CASE (17856-1190-2) / 1 mL in 1 SYRINGE", "package_ndc": "17856-1190-2", "marketing_start_date": "20250821"}], "brand_name": "Metoclopramide", "product_id": "17856-1190_3ce771f8-a078-c4ca-e063-6294a90ae2b2", "dosage_form": "SOLUTION", "pharm_class": ["Dopamine D2 Antagonists [MoA]", "Dopamine-2 Receptor Antagonist [EPC]"], "product_ndc": "17856-1190", "generic_name": "Metoclopramide", "labeler_name": "ATLANTIC BIOLOGICALS CORP.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Metoclopramide", "active_ingredients": [{"name": "METOCLOPRAMIDE HYDROCHLORIDE", "strength": "5 mg/5mL"}], "application_number": "ANDA071402", "marketing_category": "ANDA", "marketing_start_date": "20150518", "listing_expiration_date": "20261231"}