Drizalma Sprinkle - Duloxetine 40 mg / 1 Capsule 1000 Capsule, Delayed Release

Reference details for licensed healthcare facility review and verification.

NDC 1147335-0618-10
Product NDC47335-0618
Generic Drug NameDuloxetine
Brand NameDrizalma Sprinkle
ManufacturerSun Pharmaceutical Industries, Inc.
Strength40 mg / 1
Dosage FormCapsule
Drug TypeOral
Package Quantity1000 Capsule, Delayed Release
Package Description1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (47335-618-10)
Active IngredientsDuloxetine Hydrochloride
Marketing CategoryNDA

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NDC snapshot

Duloxetine 40 mg / 1 Capsule is tracked under NDC 47335-0618-10 and rolls up into product family 47335-0618. Use this page to review package-level identifiers before comparing related family pages or starting a quote review.

  • Package configuration: 1000 Capsule, Delayed Release.
  • Manufacturer: Sun Pharmaceutical Industries, Inc..
  • Dosage form: Capsule.
  • Family size: 4 indexed presentations.

Official references

Use official labeling and directory references to confirm presentation details while your team reviews the PRN catalog entry and related sourcing paths.

Alternate presentations in this family

These nearby package-level pages can help healthcare teams compare related packaging or presentation differences inside the same product-NDC family.

Drizalma Sprinkle - Duloxetine 40 mg / 1 Capsule 1000 Capsule, Delayed Release, NDC 47335-0618-10, is a Sun Pharmaceutical Industries, Inc. 40 mg / 1 capsule presentation packaged as 1000 Capsule, Delayed Release.

NDC search formats

  • Canonical NDC 11: 47335-0618-10
  • Digits-only NDC 11: 47335061810
  • Possible 10-digit display format: 47335-618-10 (4733561810)

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