NDC codes

FDA NDC Directory
Product NDC (as listed)70518-1244Labeler and product segments. Claims need a package NDC.
Product NDC at billing width70518-1244Add 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
70518-1244-07051812440030 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK (70518-1244-0)Marketed from Jun 5, 2018
70518-1244-17051812440160 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (70518-1244-1)Marketed from Mar 24, 2025
70518-1244-37051812440330 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK (70518-1244-3)Marketed from Dec 9, 2025
70518-1244-47051812440450 POUCH in 1 BOX (70518-1244-4) / 1 CAPSULE, DELAYED RELEASE in 1 POUCH (70518-1244-5)Marketed from May 17, 2026
70518-1244-67051812440650 POUCH in 1 BOX (70518-1244-6) / 1 CAPSULE, DELAYED RELEASE in 1 POUCH (70518-1244-7)Marketed from Jul 6, 2026
70518-1244-87051812440890 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (70518-1244-8)Marketed from Aug 5, 2026
70518-1244-97051812440930 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (70518-1244-9)Marketed from Aug 10, 2026

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)
Duloxetine
Generic name (nonproprietary)
duloxetine
Active ingredients
Duloxetine hydrochloride — 60 mg/1
Dosage form
Capsule, Delayed release
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 090694
Marketing start
Listing expires
Other FDA classes
Norepinephrine Uptake Inhibitors (Mechanism)Serotonin Uptake Inhibitors (Mechanism)
Identifiers
Product ID 70518-1244_58b4ec4f-c6d3-ce06-e063-6394a90a3a05SPL ID 58b4ec4f-c6d3-ce06-e063-6394a90a3a05SPL set ID 461d769c-b787-4bc7-b4a6-7a5f33ae9d45RxCUI 596934UNII 9044SC542W

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

N470518124400 followed by a unit qualifier and the quantity

Package 70518-1244-00. 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)

Duloxetine delayed-release capsule is a serotonin and norepinephrine reuptake inhibitor (SNRI) indicated for the treatment of the following conditions: Major depressive disorder (MDD) in adults ( 1 ) Generalized anxiety disorder (GAD) in adults and pediatric patients 7 years of age and older ( 1 ) Diabetic peripheral neuropathic Pain (DPNP) in adults ( 1 ) Fibromyalgia (FM) in adults and pediatric patients 13 years of age and older ( 1 ) Chronic musculoskeletal pain in adults ( 1 ) 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 periphera…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

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
ProductStrengthForm · routeLabelerProduct NDC
DuloxetineDuloxetine hydrochloride 20 mg/1Capsule, Delayed releaseOralA-S Medication Solutions50090-6406
DuloxetineDuloxetine hydrochloride 20 mg/1Capsule, Delayed releaseOralBryant Ranch Prepack71335-2624
DuloxetineDuloxetine hydrochloride 40 mg/1Capsule, Delayed releaseOralPreferred Pharmaceuticals Inc.68788-8782
DuloxetineDuloxetine hydrochloride 60 mg/1Capsule, Delayed releaseOralBryant Ranch Prepack71335-2625
DuloxetineDuloxetine hydrochloride 30 mg/1Capsule, Delayed releaseOralAdvanced Rx of Tennessee, LLC80425-0441
DuloxetineDuloxetine hydrochloride 60 mg/1Capsule, Delayed releaseOralA-S Medication Solutions50090-7897
DuloxetineDuloxetine hydrochloride 60 mg/1Capsule, Delayed releaseOralQPharma, Inc.42708-196
DuloxetineDuloxetine hydrochloride 60 mg/1Capsule, Delayed releaseOralA-S Medication Solutions50090-6775
DuloxetineDuloxetine hydrochloride 60 mg/1Capsule, Delayed releaseOralBryant Ranch Prepack71335-3163
DuloxetineDuloxetine hydrochloride 30 mg/1Capsule, Delayed releaseOralPreferred Pharmaceuticals Inc.68788-8608
DuloxetineDuloxetine hydrochloride 60 mg/1Capsule, Delayed releaseOralPreferred Pharmaceuticals Inc.68788-8623
DuloxetineDuloxetine hydrochloride 30 mg/1Capsule, Delayed releaseOralCoupler LLC67046-1585
DuloxetineDuloxetine hydrochloride 60 mg/1Capsule, Delayed releaseOralGolden State Medical Supply, Inc.51407-810
DuloxetineDuloxetine hydrochloride 60 mg/1Capsule, Delayed releaseOralCoupler LLC67046-1598
DuloxetineDuloxetine hydrochloride 20 mg/1Capsule, Delayed releaseOralGolden State Medical Supply, Inc.51407-807
DuloxetineDuloxetine hydrochloride 30 mg/1Capsule, Delayed releaseOralGolden State Medical Supply, Inc.51407-808
DuloxetineDuloxetine hydrochloride 40 mg/1Capsule, Delayed releaseOralGolden State Medical Supply, Inc.51407-809
DuloxetineDuloxetine hydrochloride 20 mg/1Capsule, Delayed releaseOralLupin Pharmaceuticals, Inc.68180-294
DuloxetineDuloxetine hydrochloride 30 mg/1Capsule, Delayed releaseOralLupin Pharmaceuticals, Inc.68180-295
DuloxetineDuloxetine hydrochloride 60 mg/1Capsule, Delayed releaseOralLupin Pharmaceuticals, Inc.68180-296

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