Duloxetine, Delayed-Release - Duloxetine Hydrochloride, Delayed-Release 40 mg / 1 Capsule 1000 Capsule, Delayed Release Pellets

Reference details for licensed healthcare facility review and verification.

NDC 1151991-0750-10
Product NDC51991-0750
Generic Drug NameDuloxetine Hydrochloride, Delayed-Release
Brand NameDuloxetine, Delayed-Release
ManufacturerBreckenridge Pharmaceutical, Inc.
Strength40 mg / 1
Dosage FormCapsule
Drug TypeOral
Package Quantity1000 Capsule, Delayed Release Pellets
Package Description1000 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (51991-750-10)
Active IngredientsDuloxetine Hydrochloride
Marketing CategoryANDA

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NDC snapshot

Duloxetine Hydrochloride, Delayed-Release 40 mg / 1 Capsule is tracked under NDC 51991-0750-10 and rolls up into product family 51991-0750. Use this page to review package-level identifiers before comparing related family pages or starting a quote review.

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

Official references

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Alternate presentations in this family

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Duloxetine, Delayed-Release - Duloxetine Hydrochloride, Delayed-Release 40 mg / 1 Capsule 1000 Capsule, Delayed Release Pellets, NDC 51991-0750-10, is a Breckenridge Pharmaceutical, Inc. 40 mg / 1 capsule presentation packaged as 1000 Capsule, Delayed Release Pellets.

NDC search formats

  • Canonical NDC 11: 51991-0750-10
  • Digits-only NDC 11: 51991075010
  • Possible 10-digit display format: 51991-750-10 (5199175010)

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