What is NDC 17856-1190?

17856-1190 is the product NDC for Metoclopramide, Metoclopramide hydrochloride 5 mg/5mL solution, listed with the FDA by ATLANTIC BIOLOGICALS CORP.. It has 2 package NDCs, shown above in 10- and 11-digit form.

ATLANTIC BIOLOGICALS CORP., NDC labeler code 17856. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Metoclopramide?

71 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Metoclopramide NDC 17856-1190 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)17856-1190Labeler and product segments. Claims need a package NDC.

Product NDC at billing width17856-1190Add the package segment from the table below.

Package NDCs as listed with the FDA, and the 11-digit 5-4-2 form used on claims. The highlighted digit is the added leading zero.
Package NDC	11-digit (billing)	Package	Copy
17856-1190-1	1785611900117856119001	72 CUP, UNIT-DOSE in 1 CASE (17856-1190-1) / 5 mL in 1 CUP, UNIT-DOSEMarketed from Aug 21, 2025
17856-1190-2	1785611900217856119002	120 SYRINGE in 1 CASE (17856-1190-2) / 1 mL in 1 SYRINGEMarketed from Aug 21, 2025

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules

Product information

Brand name (proprietary): Metoclopramide
Generic name (nonproprietary): metoclopramide
Active ingredients: Metoclopramide hydrochloride — 5 mg/5mL
Dosage form: Solution
Route: Oral
Labeler: ATLANTIC BIOLOGICALS CORP.NDC labeler code 17856
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 071402
Marketing start: May 18, 2015
Listing expires: Dec 31, 2026
Other FDA classes: Dopamine D2 Antagonists (Mechanism)
Identifiers: Product ID 17856-1190_3ce771f8-a078-c4ca-e063-6294a90ae2b2SPL ID 3ce771f8-a078-c4ca-e063-6294a90ae2b2SPL set ID 3ce3245f-7021-5135-e063-6394a90a7d95RxCUI 104884UNII W1792A2RVD
Pharmacologic class: Dopamine-2 Receptor Antagonist

Billing references

What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.

HCPCS codeNo match

No HCPCS code in Med-Code's directory. Oral products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N417856119001 followed by a unit qualifier and the quantity

Package 17856-1190-01. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier

Product label

Current FDA label (SPL), effective Oct 30, 2026. This label includes a boxed warning.

Indications (excerpt from the label)

INDICATIONS AND USAGE The use of Metoclopramide Oral Solution is recommended for adults only. Therapy should not exceed 12 weeks in duration. Symptomatic Gastroesophageal Reflux Metoclopramide Oral Solution is indicated as short-term (4 to 12 weeks) therapy for adults with symptomatic, documented gastroesophageal reflux who fail to respond to conventional therapy. The principal effect of metoclopramide is on symptoms of post-prandial and daytime heartburn with less observed effect on nocturnal symptoms. If symptoms are confined to particular situations, such as following the evening meal, use of metoclopramide as single doses prior to the provocative situation should be considered, rather th…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 17856-1190

What is NDC 17856-1190?: 17856-1190 is the product NDC for Metoclopramide, Metoclopramide hydrochloride 5 mg/5mL solution, listed with the FDA by ATLANTIC BIOLOGICALS CORP.. It has 2 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Metoclopramide.
What is the active ingredient?: Metoclopramide hydrochloride.
Who is the labeler?: ATLANTIC BIOLOGICALS CORP., NDC labeler code 17856. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Metoclopramide?: 71 other product NDCs are listed under this name. See all Metoclopramide NDCs.
Is there a related HCPCS / J-code?: Not in Med-Code's curated HCPCS directory. See Billing references above.

Other finished products listed under the same name: strengths, forms and labelers.

Other Metoclopramide NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Metoclopramide	Metoclopramide hydrochloride 5 mg/mL	Injection, SolutionIntramuscular, Intravenous	Baxter Healthcare Corporation	36000-366	36000-0366-25
Metoclopramide	Metoclopramide hydrochloride 5 mg/1	TabletOral	Coupler LLC	67046-0186	67046-0186-03
Metoclopramide	Metoclopramide hydrochloride 10 mg/1	TabletOral	Coupler LLC	67046-0581	67046-0581-03
Metoclopramidemetoclopramide hydrochloride	Metoclopramide hydrochloride 5 mg/mL	InjectionIntramuscular, Intravenous	Henry Schein, Inc.	0404-9771	00404-9771-02
Metoclopramide	Metoclopramide hydrochloride 5 mg/1	TabletOral	Safecor Health LLC	48433-066	48433-0066-20
Metoclopramide	Metoclopramide hydrochloride 10 mg/1	TabletOral	Safecor Health LLC	48433-067	48433-0067-20
Metoclopramide	Metoclopramide hydrochloride 10 mg/1	TabletOral	REMEDYREPACK INC.	70518-4541	70518-4541-00
Metoclopramide	Metoclopramide hydrochloride 5 mg/mL	Injection, SolutionIntramuscular, Intravenous	Cardinal Health 107, LLC	55154-7832	55154-7832-05
Metoclopramide	Metoclopramide hydrochloride 5 mg/1	TabletOral	ScieGen Pharmaceuticals, Inc.	50228-232	50228-0232-0150228-0232-05
Metoclopramide	Metoclopramide hydrochloride 10 mg/1	TabletOral	ScieGen Pharmaceuticals, Inc.	50228-233	50228-0233-0150228-0233-0550228-0233-10

All 72 Metoclopramide NDCs

Other NDCs under ANDA 071402

Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.

FDA NDC Directory listings under ANDA 071402
Product	Strength	Form · route	Labeler	Product NDC
Metoclopramide	Metoclopramide hydrochloride 5 mg/5mL	SolutionOral	American Health Packaging	60687-837
Metoclopramide	Metoclopramide hydrochloride 5 mg/5mL	SolutionOral	ANI Pharmaceuticals, Inc.	62559-190
Metoclopramide	Metoclopramide hydrochloride 5 mg/5mL	SolutionOral	Bryant Ranch Prepack	63629-1961
Metoclopramide	Metoclopramide hydrochloride 5 mg/5mL	SolutionOral	Bryant Ranch Prepack	63629-2144
Metoclopramide	Metoclopramide hydrochloride 5 mg/5mL	SolutionOral	Bryant Ranch Prepack	71335-2732
Metoclopramide	Metoclopramide hydrochloride 5 mg/5mL	SolutionOral	Bryant Ranch Prepack	71335-2997
Metoclopramide	Metoclopramide hydrochloride 5 mg/5mL	SolutionOral	Bryant Ranch Prepack	72162-1750