Sertraline Hydrochloride NDC 87441-075

Product information

Brand name (proprietary)

Sertraline Hydrochloride

Generic name (nonproprietary)

sertraline hydrochloride

Active ingredients

Sertraline hydrochloride — 25 mg/1

Dosage form

Tablet, Film coated

Route

Oral

Labeler

Unit Dose Solutions, Inc.

Product type

Prescription drug

Marketing category

ANDA — Abbreviated New Drug Application (generic)Application ANDA 077670

Marketing start

Jul 6, 2026

Listing expires

Dec 31, 2027

Other FDA classes

Cytochrome P450 2D6 Inhibitors (Mechanism)Serotonin Uptake Inhibitors (Mechanism)

Identifiers

Product ID 87441-075_55f514c6-f6ed-13ac-e063-6294a90ac957SPL ID 55f514c6-f6ed-13ac-e063-6294a90ac957SPL set ID 55f514c6-f6ec-13ac-e063-6294a90ac957RxCUI 312940UNII UTI8907Y6X

Pharmacologic class

Serotonin 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

N487441007501 followed by a unit qualifier and the quantity Copy

Package 87441-0075-01. 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

Label details couldn’t be retrieved right now. Open the label on DailyMed.

Other NDCs under ANDA 077670

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

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