Duloxetine - Hydrochloride 40 mg / 1 Capsule 90 Capsule, Delayed Release Pellets

Reference details for licensed healthcare facility review and verification.

Duloxetine Hydrochloride NDC Family 82009-0031 Duloxetine Hydrochloride 40 mg / 1

NDC 11	82009-0031-90
Product NDC	82009-0031
Generic Drug Name	Duloxetine Hydrochloride
Brand Name	Duloxetine
Manufacturer	Quallent Pharmaceuticals Health, LLC
Strength	40 mg / 1
Dosage Form	Capsule
Drug Type	Oral
Package Quantity	90 Capsule, Delayed Release Pellets
Package Description	90 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (82009-031-90)
Active Ingredients	Duloxetine Hydrochloride
Marketing Category	ANDA

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NDC snapshot

Duloxetine Hydrochloride 40 mg / 1 Capsule is tracked under NDC 82009-0031-90 and rolls up into product family 82009-0031. Use this page to review package-level identifiers before comparing related family pages or starting a quote review.

Package configuration: 90 Capsule, Delayed Release Pellets.
Manufacturer: Quallent Pharmaceuticals Health, 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 40 mg / 1 Capsule 90 Capsule, Delayed Release Pellets, NDC 82009-0031-90, is a Quallent Pharmaceuticals Health, LLC 40 mg / 1 capsule presentation packaged as 90 Capsule, Delayed Release Pellets.

NDC search formats

Canonical NDC 11: 82009-0031-90
Digits-only NDC 11: 82009003190
Possible 10-digit display format: 82009-031-90 (8200903190)

Helpful product links

Search by brand name: Duloxetine
NDC 11: 82009-0031-90
Product family NDC: 82009-0031
VA classification code: CN609
VA classification code description: ANTIDEPRESSANTS,OTHER
CMOP ID: D1104
VUID: 4034655