Duloxetine NDC 87063-702

Product information

Brand name (proprietary)

Duloxetine

Generic name (nonproprietary)

duloxetine

Active ingredients

Duloxetine hydrochloride — 20 mg/1

Dosage form

Capsule, Delayed release

Route

Oral

Labeler

ASCLEMED USA INC.NDC labeler code 87063

Product type

Prescription drug

Marketing category

ANDA — Abbreviated New Drug Application (generic)Application ANDA 208706

Marketing start

Mar 16, 2017

Listing expires

Dec 31, 2027

Other FDA classes

Norepinephrine Uptake Inhibitors (Mechanism)Serotonin Uptake Inhibitors (Mechanism)

Identifiers

Product ID 87063-702_559e1f92-2c7f-590f-e063-6294a90a52efSPL ID 559e1f92-2c7f-590f-e063-6294a90a52ef

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

N487063070212 followed by a unit qualifier and the quantity Copy

Package 87063-0702-12. 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

The FDA listing for this product does not reference a label (SPL) set.

About NDC 87063-702

What is NDC 87063-702?

87063-702 is the product NDC for Duloxetine, Duloxetine hydrochloride 20 mg/1 capsule, delayed release, listed with the FDA by ASCLEMED USA INC.. It has 4 package NDCs, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

Duloxetine.

What is the active ingredient?

Duloxetine hydrochloride.

Who is the labeler?

ASCLEMED USA INC., NDC labeler code 87063. 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?

140 other product NDCs are listed under this name. See all Duloxetine NDCs.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory. See Billing references above.

Related NDCs: other Duloxetine products

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

All 141 Duloxetine NDCs

Other NDCs under ANDA 208706

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

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