Duloxetine 30 mg / 1 Capsule 105 Capsule, Delayed Release

Reference details for licensed healthcare facility review and verification.

NDC 1131722-0169-32
Product NDC31722-0169
Generic Drug NameDuloxetine
Brand NameDuloxetine
ManufacturerCamber Pharmaceuticals, Inc.
Strength30 mg / 1
Dosage FormCapsule
Drug TypeOral
Package Quantity105 Capsule, Delayed Release
Package Description105 CAPSULE, DELAYED RELEASE in 1 CARTON (31722-169-32)
Active IngredientsDuloxetine Hydrochloride
Marketing CategoryANDA

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NDC snapshot

Duloxetine 30 mg / 1 Capsule is tracked under NDC 31722-0169-32 and rolls up into product family 31722-0169. Use this page to review package-level identifiers before comparing related family pages or starting a quote review.

  • Package configuration: 105 Capsule, Delayed Release.
  • Manufacturer: Camber Pharmaceuticals, Inc..
  • Dosage form: Capsule.
  • Family size: 6 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 30 mg / 1 Capsule 105 Capsule, Delayed Release, NDC 31722-0169-32, is a Camber Pharmaceuticals, Inc. 30 mg / 1 capsule presentation packaged as 105 Capsule, Delayed Release.

NDC search formats

  • Canonical NDC 11: 31722-0169-32
  • Digits-only NDC 11: 31722016932
  • Possible 10-digit display format: 31722-169-32 (3172216932)

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