NDC codes

FDA NDC Directory
Product NDC (as listed)30698-456Labeler and product segments. Claims need a package NDC.
Product NDC at billing width30698-0456Add 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 NDC11-digit (billing)PackageCopy
30698-456-0230698045602306980456021 BOTTLE, GLASS in 1 CARTON (30698-456-02) / 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)
Atoncy
Generic name (nonproprietary)
atomoxetine hydrochloride
Active ingredients
Atomoxetine hydrochloride — 4 mg/mL
Dosage form
Solution
Route
Oral
Labeler
Validus Pharmaceuticals LLCNDC labeler code 30698
Product type
Prescription drug
Marketing category
NDA — New Drug ApplicationApplication NDA 220320
Marketing start
Listing expires
Other FDA classes
Norepinephrine Uptake Inhibitors (Mechanism)
Identifiers
Product ID 30698-456_4e746d28-ff24-2255-e063-6294a90a2c71SPL ID 4e746d28-ff24-2255-e063-6294a90a2c71SPL set ID 72d3d8cf-7f3b-479e-bd9f-e204d4118517RxCUI 2739831, 2739837UNII 57WVB6I2W0UPC 0330698456026
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

N430698045602 followed by a unit qualifier and the quantity

Package 30698-0456-02. 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 . This label includes a boxed warning.

Indications (excerpt from the label)

ATONCY is indicated for the treatment of attention-deficit/hyperactivity disorder (ADHD) in adult and pediatric patients 6 years of age and older. ATONCY 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. ATONCY 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 30698-456

What is NDC 30698-456?
30698-456 is the product NDC for Atoncy (atomoxetine hydrochloride), Atomoxetine hydrochloride 4 mg/mL solution, listed with the FDA by Validus Pharmaceuticals LLC. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Atoncy (Atomoxetine hydrochloride).
What is the active ingredient?
Atomoxetine hydrochloride.
Who is the labeler?
Validus Pharmaceuticals LLC, NDC labeler code 30698. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Atoncy?
None: this is the only finished product listed under this name.
Is there a related HCPCS / J-code?
Not in Med-Code's curated HCPCS directory. See Billing references above.

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
ProductStrengthForm · routeLabelerProduct NDC
Atomoxetine hydrochlorideAtomoxetine hydrochloride 4 mg/mLSolutionOralAdvagen Pharma Ltd.72888-456

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