Duloxetine Hydrochloride 20 mg / 1 Capsule 60 Capsule, Delayed Release Pellets

Reference details for licensed healthcare facility review and verification.

NDC 1150771-0201-01
Product NDC50771-0201
Generic Drug NameDuloxetine Hydrochloride
Brand NameDuloxetine Hydrochloride
ManufacturerYaopharma Co., Ltd.
Strength20 mg / 1
Dosage FormCapsule
Drug TypeOral
Package Quantity60 Capsule, Delayed Release Pellets
Package Description60 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE, PLASTIC (50771-201-01)
Active IngredientsDuloxetine Hydrochloride
Marketing CategoryANDA

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NDC snapshot

Duloxetine Hydrochloride 20 mg / 1 Capsule is tracked under NDC 50771-0201-01 and rolls up into product family 50771-0201. Use this page to review package-level identifiers before comparing related family pages or starting a quote review.

  • Package configuration: 60 Capsule, Delayed Release Pellets.
  • Manufacturer: Yaopharma Co., Ltd..
  • Dosage form: Capsule.
  • Family size: 1 indexed presentation.

Official references

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

Duloxetine Hydrochloride 20 mg / 1 Capsule 60 Capsule, Delayed Release Pellets, NDC 50771-0201-01, is a Yaopharma Co., Ltd. 20 mg / 1 capsule presentation packaged as 60 Capsule, Delayed Release Pellets.

NDC search formats

  • Canonical NDC 11: 50771-0201-01
  • Digits-only NDC 11: 50771020101
  • Possible 10-digit display formats: 50771-201-01 (5077120101), 50771-0201-1 (5077102011)

Multiple 10-digit display-format aliases can map to the same stored 11-digit billing NDC, so these are shown as search aliases rather than a single asserted package format.

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