Fenofibric Acid 135 mg / 1 Capsule 90 Capsule, Delayed Release

Reference details for licensed healthcare facility review and verification.

Fenofibric Acid NDC Family 59651-0217 Fenofibric Acid 135 mg / 1

NDC 11	59651-0217-90
Product NDC	59651-0217
Generic Drug Name	Fenofibric Acid
Brand Name	Fenofibric Acid
Manufacturer	Aurobindo Pharma Limited
Strength	135 mg / 1
Dosage Form	Capsule
Drug Type	Oral
Package Quantity	90 Capsule, Delayed Release
Package Description	90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (59651-217-90)
Active Ingredients	Fenofibric Acid
Marketing Category	ANDA

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NDC snapshot

Fenofibric Acid 135 mg / 1 Capsule is tracked under NDC 59651-0217-90 and rolls up into product family 59651-0217. Use this page to review package-level identifiers before comparing related family pages or starting a quote review.

Package configuration: 90 Capsule, Delayed Release.
Manufacturer: Aurobindo Pharma Limited.
Dosage form: Capsule.
Family size: 1 indexed presentation.

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Review the generic familyFenofibric Acid

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Potential alternatives with matching presentation

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View Potential Alternative HubFenofibric acid 135 mg / 1 Capsule delayed release 90 Capsule, Delayed Release Bottle9 package-level listings in the comparison hub.

Sample package-level pages in this comparison set

Fenofibric Acid 135 mg / 1 Capsule 90 Capsule, Delayed Release, NDC 59651-0217-90, is a Aurobindo Pharma Limited 135 mg / 1 capsule presentation packaged as 90 Capsule, Delayed Release.

NDC search formats

Canonical NDC 11: 59651-0217-90
Digits-only NDC 11: 59651021790
Possible 10-digit display format: 59651-217-90 (5965121790)

Helpful product links

Search by brand name: Fenofibric Acid
NDC 11: 59651-0217-90
Product family NDC: 59651-0217
VA classification code: CV350
VA classification code description: ANTILIPEMIC AGENTS
CMOP ID: F0430
VUID: 4028323