What is NDC 72189-615?

72189-615 is the product NDC for Duloxetine D/R, Duloxetine hydrochloride 30 mg/1 capsule, delayed release, listed with the FDA by Direct_Rx. It has 3 package NDCs, shown above in 10- and 11-digit form.

Direct_Rx, NDC labeler code 72189. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Duloxetine D/R?

3 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Duloxetine D/R NDC 72189-615 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)72189-615Labeler and product segments. Claims need a package NDC.

Product NDC at billing width72189-0615Add 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
72189-615-30	7218906153072189061530	30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (72189-615-30)Marketed from Feb 17, 2025
72189-615-60	7218906156072189061560	60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (72189-615-60)Marketed from Feb 17, 2025
72189-615-90	7218906159072189061590	90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (72189-615-90)Marketed from Feb 17, 2025

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): Duloxetine D/R
Generic name (nonproprietary): duloxetine d/r
Active ingredients: Duloxetine hydrochloride — 30 mg/1
Dosage form: Capsule, Delayed release
Route: Oral
Labeler: Direct_RxNDC labeler code 72189
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 090694
Marketing start: Feb 17, 2025
Listing expires: Dec 31, 2026
Other FDA classes: Norepinephrine Uptake Inhibitors (Mechanism)Serotonin Uptake Inhibitors (Mechanism)
Identifiers: Product ID 72189-615_35ced01c-03fc-4779-e063-6394a90a9cd5SPL ID 35ced01c-03fc-4779-e063-6394a90a9cd5SPL set ID 2e58add7-b85e-2772-e063-6294a90a580dRxCUI 596930UNII 9044SC542W
Pharmacologic class: Serotonin and 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

N472189061530 followed by a unit qualifier and the quantity

Package 72189-0615-30. 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 May 23, 2025. This label includes a boxed warning.

Indications (excerpt from the label)

Duloxetine delayed-release capsules are indicated for the treatment of: Major depressive disorder in adults Generalized anxiety disorder in adults and pediatric patients 7 years of age and older Diabetic peripheral neuropathic pain in adults Fibromyalgia in adults and pediatric patients 13 years of age and older Chronic musculoskeletal pain in adults

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 72189-615

What is NDC 72189-615?: 72189-615 is the product NDC for Duloxetine D/R, Duloxetine hydrochloride 30 mg/1 capsule, delayed release, listed with the FDA by Direct_Rx. It has 3 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Duloxetine D/R.
What is the active ingredient?: Duloxetine hydrochloride.
Who is the labeler?: Direct_Rx, NDC labeler code 72189. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Duloxetine D/R?: 3 other product NDCs are listed under this name. See all Duloxetine D/R 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 Duloxetine D/R NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Duloxetine D/R	Duloxetine hydrochloride 30 mg/1	Capsule, Delayed releaseOral	Direct_Rx	72189-661	72189-0661-3072189-0661-60
Duloxetine D/R	Duloxetine hydrochloride 20 mg/1	Capsule, Delayed releaseOral	Direct_Rx	72189-634	72189-0634-30
Duloxetine D/R	Duloxetine hydrochloride 60 mg/1	Capsule, Delayed releaseOral	Direct_Rx	72189-608	72189-0608-3072189-0608-6072189-0608-90

Other NDCs under ANDA 090694

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

FDA NDC Directory listings under ANDA 090694
Product	Strength	Form · route	Labeler	Product NDC
Duloxetine	Duloxetine hydrochloride 20 mg/1	Capsule, Delayed releaseOral	NCS HealthCare of KY, LLC dba Vangard Labs	0615-8494
Duloxetine	Duloxetine hydrochloride 30 mg/1	Capsule, Delayed releaseOral	NCS HealthCare of KY, LLC dba Vangard Labs	0615-8495
Duloxetine	Duloxetine hydrochloride 60 mg/1	Capsule, Delayed releaseOral	NCS HealthCare of KY, LLC dba Vangard Labs	0615-8496
Duloxetine	Duloxetine hydrochloride 60 mg/1	Capsule, Delayed releaseOral	QPharma, Inc.	42708-196
Duloxetine	Duloxetine hydrochloride 30 mg/1	Capsule, Delayed releaseOral	A-S Medication Solutions	50090-6281
Duloxetine	Duloxetine hydrochloride 20 mg/1	Capsule, Delayed releaseOral	A-S Medication Solutions	50090-6406
Duloxetine	Duloxetine hydrochloride 60 mg/1	Capsule, Delayed releaseOral	A-S Medication Solutions	50090-6775
Duloxetine	Duloxetine hydrochloride 30 mg/1	Capsule, Delayed releaseOral	A-S Medication Solutions	50090-7784
Duloxetine	Duloxetine hydrochloride 60 mg/1	Capsule, Delayed releaseOral	A-S Medication Solutions	50090-7897
Duloxetine	Duloxetine hydrochloride 20 mg/1	Capsule, Delayed releaseOral	Golden State Medical Supply, Inc.	51407-807
Duloxetine	Duloxetine hydrochloride 30 mg/1	Capsule, Delayed releaseOral	Golden State Medical Supply, Inc.	51407-808
Duloxetine	Duloxetine hydrochloride 40 mg/1	Capsule, Delayed releaseOral	Golden State Medical Supply, Inc.	51407-809
Duloxetine	Duloxetine hydrochloride 60 mg/1	Capsule, Delayed releaseOral	Golden State Medical Supply, Inc.	51407-810
Duloxetine	Duloxetine hydrochloride 30 mg/1	Capsule, Delayed releaseOral	Coupler LLC	67046-1585
Duloxetine	Duloxetine hydrochloride 60 mg/1	Capsule, Delayed releaseOral	Coupler LLC	67046-1598
Duloxetine	Duloxetine hydrochloride 60 mg/1	Capsule, Delayed releaseOral	NuCare Pharmaceuticals, Inc.	68071-3775
Duloxetine	Duloxetine hydrochloride 20 mg/1	Capsule, Delayed releaseOral	Lupin Pharmaceuticals, Inc.	68180-294
Duloxetine	Duloxetine hydrochloride 30 mg/1	Capsule, Delayed releaseOral	Lupin Pharmaceuticals, Inc.	68180-295
Duloxetine	Duloxetine hydrochloride 60 mg/1	Capsule, Delayed releaseOral	Lupin Pharmaceuticals, Inc.	68180-296
Duloxetine	Duloxetine hydrochloride 40 mg/1	Capsule, Delayed releaseOral	Lupin Pharmaceuticals, Inc.	68180-297

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