382 382 Pill — WHITE;BLUE CAPSULE, 16mm — Duloxetine

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Imprint382 / 382
ColourWHITE;BLUE
ShapeCAPSULE
Size16
StrengthDULOXETINE HYDROCHLORIDE 30 mg
Dosage formCapsule, Delayed Release
ManufacturerSun Pharmaceutical Industries, Inc
NDC47335-382
Schedule—
AvailabilityPrescription only
IngredientsDULOXETINE HYDROCHLORIDE[DULOXETINE]

What does this imprint mean?

The imprint "382 382" is a code stamped or printed on the tablet or capsule by the manufacturer, used to identify the drug, its strength and the maker.

Active ingredient

Duloxetine

Uses and warnings

BOXED WARNING: "Antidepressants increased the risk of suicidal thoughts and behavior in children, adolescents, and young adults in short-term studies." Monitoring is essential during treatment initiation and dose changes. Key Precautions Include: - Hepatotoxicity: Risk of liver failure; avoid in chronic liver disease or cirrhosis - Orthostatic Hypotension & Falls: May cause blood pressure drops and syncope, particularly in elderly patients - Serotonin Syndrome: Dangerous interaction risk with MAOIs and other serotonergic drugs - Abnormal Bleeding: Increased bleeding risk, especially with NSAIDs or anticoagulants - Discontinuation Symptoms: Gradual dose reduction recommended to avoid dizziness, headache, nausea - Severe Skin Reactions: Stevens-Johnson Syndrome possible; discontinue at first sign - Angle-Closure Glaucoma: May trigger attacks in susceptible patients - Blood Pressure Monitoring: Required before and during treatment ---

Duloxetine delayed-release capsules are indicated for treating: "Major Depressive Disorder (MDD)," "Generalized Anxiety Disorder (GAD)," "Diabetic Peripheral Neuropathy," and "Chronic Musculoskeletal Pain." ---

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Official references

Source: FDA Structured Product Label via NLM Pillbox archive (retired 2021); source file e92e215f-73c5-49a4-b2a0-d3b40d3bea47.xml