Duloxetine - Hydrochloride 20 mg / 1 Capsule 3600 Capsule, Delayed Release

Reference details for licensed healthcare facility review and verification.

Duloxetine Hydrochloride NDC Family 71610-0401 Duloxetine Hydrochloride 20 mg / 1

NDC 11	71610-0401-83
Product NDC	71610-0401
Generic Drug Name	Duloxetine Hydrochloride
Brand Name	Duloxetine
Manufacturer	Aphena Pharma Solutions - Tennessee, LLC
Strength	20 mg / 1
Dosage Form	Capsule
Drug Type	Oral
Package Quantity	3600 Capsule, Delayed Release
Package Description	3600 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71610-401-83)
Active Ingredients	Duloxetine Hydrochloride
Marketing Category	ANDA

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NDC snapshot

Duloxetine Hydrochloride 20 mg / 1 Capsule is tracked under NDC 71610-0401-83 and rolls up into product family 71610-0401. Use this page to confirm the exact presentation before comparing related family pages or starting a quote review.

Package configuration: 3600 Capsule, Delayed Release.
Manufacturer: Aphena Pharma Solutions - Tennessee, LLC.
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 3600 Capsule, Delayed Release, NDC 71610-0401-83, is a Aphena Pharma Solutions - Tennessee, LLC 20 mg / 1 capsule presentation packaged as 3600 Capsule, Delayed Release.

NDC search formats

Canonical NDC 11: 71610-0401-83
Digits-only NDC 11: 71610040183
Possible 10-digit display format: 71610-401-83 (7161040183)

Helpful product links

Search by brand name: Duloxetine
Exact NDC 11: 71610-0401-83
Product family NDC: 71610-0401
VA classification code: CN609
VA classification code description: ANTIDEPRESSANTS,OTHER
CMOP ID: D0922
VUID: 4031191