Venlafaxine hydrochloride 37.5 mg / 1 Tablet 30 Tablet, Extended Release

Reference details for licensed healthcare facility review and verification.

venlafaxine hydrochloride NDC Family 68025-0079 venlafaxine hydrochloride 37.5 mg / 1

NDC 11	68025-0079-30
Product NDC	68025-0079
Generic Drug Name	venlafaxine hydrochloride
Brand Name	Venlafaxine Hydrochloride
Manufacturer	Vertical Pharmaceuticals, LLC
Strength	37.5 mg / 1
Dosage Form	Tablet
Drug Type	Oral
Package Quantity	30 Tablet, Extended Release
Package Description	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (68025-079-30)
Active Ingredients	Venlafaxine Hydrochloride
Marketing Category	NDA AUTHORIZED GENERIC

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NDC snapshot

venlafaxine hydrochloride 37.5 mg / 1 Tablet is tracked under NDC 68025-0079-30 and rolls up into product family 68025-0079. Use this page to confirm the exact presentation before comparing related family pages or starting a quote review.

Package configuration: 30 Tablet, Extended Release.
Manufacturer: Vertical Pharmaceuticals, LLC.
Dosage form: Tablet.
Family size: 1 indexed presentation.

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Review the generic familyvenlafaxine hydrochloride

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Venlafaxine hydrochloride 37.5 mg / 1 Tablet 30 Tablet, Extended Release, NDC 68025-0079-30, is a Vertical Pharmaceuticals, LLC 37.5 mg / 1 tablet presentation packaged as 30 Tablet, Extended Release.

NDC search formats

Canonical NDC 11: 68025-0079-30
Digits-only NDC 11: 68025007930
Possible 10-digit display format: 68025-079-30 (6802507930)

Helpful product links

Search by brand name: Venlafaxine Hydrochloride
Exact NDC 11: 68025-0079-30
Product family NDC: 68025-0079
VA classification code: CN609
VA classification code description: ANTIDEPRESSANTS,OTHER
CMOP ID: V0181
VUID: 4028046