metoclopramide
Generic: metoclopramide hydrochloride
Labeler: atlantic biologicals corp.Drug Facts
Product Profile
Brand Name
metoclopramide
Generic Name
metoclopramide hydrochloride
Labeler
atlantic biologicals corp.
Dosage Form
SOLUTION
Routes
Active Ingredients
metoclopramide hydrochloride 5 mg/5mL
Manufacturer
Identifiers & Regulatory
Product NDC
17856-0576
Product ID
17856-0576_3b3f252b-3f29-3484-e063-6394a90a1568
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA072744
Listing Expiration
2026-12-31
Marketing Start
1991-06-01
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
178560576
Hyphenated Format
17856-0576
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 hydrochloride (source: ndc)
Application Number
ANDA072744 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 5 mg/5mL
Packaging
- HOW SUPPLIED NDC:17856-0576-5 in a CUP of 5 SOLUTIONS Store at 20° to 25°C (68° to 77°F). [See USP Controlled Room Temperature.]
- METOCLOPRAMIDE (METOCLOPRAMIDE HYDROCHLORIDE) SOLUTION image description
Packages (0)
No package records.
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3b3f252b-3f29-3484-e063-6394a90a1568", "openfda": {"unii": ["W1792A2RVD"], "rxcui": ["104884"], "spl_set_id": ["3cd4b274-6176-4e5b-9765-4f50763bd58f"], "manufacturer_name": ["ATLANTIC BIOLOGICALS CORP."]}, "finished": true, "packaging": [], "brand_name": "Metoclopramide", "product_id": "17856-0576_3b3f252b-3f29-3484-e063-6394a90a1568", "dosage_form": "SOLUTION", "pharm_class": ["Dopamine D2 Antagonists [MoA]", "Dopamine-2 Receptor Antagonist [EPC]"], "product_ndc": "17856-0576", "generic_name": "metoclopramide hydrochloride", "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": "ANDA072744", "marketing_category": "ANDA", "marketing_start_date": "19910601", "listing_expiration_date": "20261231"}