Duloxetine 20 mg / 1 Capsule 20 Capsule, Delayed Release

Reference details for licensed healthcare facility review and verification.

NDC 1176420-0633-20
Product NDC76420-0633
Generic Drug NameDuloxetine
Brand NameDuloxetine
ManufacturerAsclemed USA, Inc.
Strength20 mg / 1
Dosage FormCapsule
Drug TypeOral
Package Quantity20 Capsule, Delayed Release
Package Description20 CAPSULE, DELAYED RELEASE in 1 BOTTLE (76420-633-20)
Active IngredientsDuloxetine Hydrochloride
Marketing CategoryANDA

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NDC snapshot

Duloxetine 20 mg / 1 Capsule is tracked under NDC 76420-0633-20 and rolls up into product family 76420-0633. Use this page to review package-level identifiers before comparing related family pages or starting a quote review.

  • Package configuration: 20 Capsule, Delayed Release.
  • Manufacturer: Asclemed USA, Inc..
  • Dosage form: Capsule.
  • Family size: 7 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.

Duloxetine 20 mg / 1 Capsule 20 Capsule, Delayed Release, NDC 76420-0633-20, is a Asclemed USA, Inc. 20 mg / 1 capsule presentation packaged as 20 Capsule, Delayed Release.

NDC search formats

  • Canonical NDC 11: 76420-0633-20
  • Digits-only NDC 11: 76420063320
  • Possible 10-digit display format: 76420-633-20 (7642063320)

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