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

Reference details for licensed healthcare facility review and verification.

Duloxetine Hydrochloride NDC Family 50771-0201 Duloxetine Hydrochloride 20 mg / 1

NDC 11	50771-0201-01
Product NDC	50771-0201
Generic Drug Name	Duloxetine Hydrochloride
Brand Name	Duloxetine Hydrochloride
Manufacturer	Yaopharma Co., Ltd.
Strength	20 mg / 1
Dosage Form	Capsule
Drug Type	Oral
Package Quantity	60 Capsule, Delayed Release Pellets
Package Description	60 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE, PLASTIC (50771-201-01)
Active Ingredients	Duloxetine Hydrochloride
Marketing Category	ANDA

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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 confirm the exact presentation 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.

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Review the generic familyDuloxetine Hydrochloride

Official references

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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.

Helpful product links

Search by brand name: Duloxetine Hydrochloride
Exact NDC 11: 50771-0201-01
Product family NDC: 50771-0201