What is NDC 72888-456?

72888-456 is the product NDC for Atomoxetine hydrochloride, Atomoxetine hydrochloride 4 mg/mL solution, listed with the FDA by Advagen Pharma Ltd.. It has 1 package NDC, shown above in 10- and 11-digit form.

Advagen Pharma Ltd., NDC labeler code 72888. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Atomoxetine hydrochloride?

19 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Atomoxetine hydrochloride NDC 72888-456

NDC codes

FDA NDC Directory

Product NDC (as listed)72888-456Labeler and product segments. Claims need a package NDC.

Product NDC at billing width72888-0456Add 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
72888-456-01	7288804560172888045601	1 BOTTLE, GLASS in 1 CARTON (72888-456-01) / 100 mL in 1 BOTTLE, GLASSMarketed from Mar 20, 2026

How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 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): Atomoxetine hydrochloride
Generic name (nonproprietary): atomoxetine hydrochloride
Active ingredients: Atomoxetine hydrochloride — 4 mg/mL
Dosage form: Solution
Route: Oral
Labeler: Advagen Pharma Ltd.NDC labeler code 72888
Product type: Prescription drug
Marketing category: NDA authorized genericApplication NDA 220320
Marketing start: Mar 20, 2026
Listing expires: Dec 31, 2027
Other FDA classes: Norepinephrine Uptake Inhibitors (Mechanism)
Identifiers: Product ID 72888-456_4e8dc87f-5d2d-5277-e063-6394a90ae95fSPL ID 4e8dc87f-5d2d-5277-e063-6394a90ae95fSPL set ID 16096e9c-2dcd-4c84-a1a8-1c85d6d6898cRxCUI 2739831UNII 57WVB6I2W0UPC 0372888456010
Pharmacologic class: Norepinephrine Reuptake Inhibitor

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

N472888045601 followed by a unit qualifier and the quantity

Package 72888-0456-01. 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 Apr 3, 2026. This label includes a boxed warning.

Indications (excerpt from the label)

Atomoxetine oral solution is indicated for the treatment of attention-deficit/hyperactivity disorder (ADHD) in adult and pediatric patients 6 years of age and older. Atomoxetine oral solution is indicated as an integral part of a total treatment program for ADHD that may include other measures (psychological, educational, social) for patients with ADHD. Atomoxetine oral solution is a selective norepinephrine reuptake inhibitor (SNRI) indicated for the treatment of ADHD in adults and pediatric patients 6 years of age and older. ( 1 )

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 72888-456

What is NDC 72888-456?: 72888-456 is the product NDC for Atomoxetine hydrochloride, Atomoxetine hydrochloride 4 mg/mL solution, listed with the FDA by Advagen Pharma Ltd.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Atomoxetine hydrochloride.
What is the active ingredient?: Atomoxetine hydrochloride.
Who is the labeler?: Advagen Pharma Ltd., NDC labeler code 72888. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Atomoxetine hydrochloride?: 19 other product NDCs are listed under this name. See all Atomoxetine hydrochloride 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 Atomoxetine hydrochloride NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Atomoxetine Hydrochloride	Atomoxetine hydrochloride 10 mg/1	CapsuleOral	REMEDYREPACK INC.	70518-4313	70518-4313-00
Atomoxetine Hydrochloride	Atomoxetine hydrochloride 60 mg/1	CapsuleOral	AvPAK	50268-059	50268-0059-13
Atomoxetine Hydrochloride	Atomoxetine hydrochloride 25 mg/1	CapsuleOral	AvPAK	50268-057	50268-0057-13
Atomoxetine Hydrochloride	Atomoxetine hydrochloride 40 mg/1	CapsuleOral	AvPAK	50268-058	50268-0058-13
Atomoxetine Hydrochloride	Atomoxetine hydrochloride 40 mg/1	CapsuleOral	A-S Medication Solutions	50090-4236	50090-4236-00
Atomoxetine Hydrochloride	Atomoxetine hydrochloride 10 mg/1	CapsuleOral	Apotex Corp.	60505-2830	60505-2830-03
Atomoxetine Hydrochloride	Atomoxetine hydrochloride 18 mg/1	CapsuleOral	Apotex Corp.	60505-2831	60505-2831-03
Atomoxetine Hydrochloride	Atomoxetine hydrochloride 25 mg/1	CapsuleOral	Apotex Corp.	60505-2832	60505-2832-03
Atomoxetine Hydrochloride	Atomoxetine hydrochloride 40 mg/1	CapsuleOral	Apotex Corp.	60505-2833	60505-2833-03
Atomoxetine Hydrochloride	Atomoxetine hydrochloride 60 mg/1	CapsuleOral	Apotex Corp.	60505-2834	60505-2834-03

All 20 Atomoxetine hydrochloride NDCs

Other NDCs under NDA 220320

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

FDA NDC Directory listings under NDA 220320
Product	Strength	Form · route	Labeler	Product NDC
Atoncyatomoxetine hydrochloride	Atomoxetine hydrochloride 4 mg/mL	SolutionOral	Validus Pharmaceuticals LLC	30698-456