Venlafaxine Hydrochloride - Venlafaxine 75 mg / 1 Tablet 90 Tablet, Extended Release

Reference details for licensed healthcare facility review and verification.

NDC 1170518-4065-00
Product NDC70518-4065
Generic Drug NameVenlafaxine
Brand NameVenlafaxine Hydrochloride
ManufacturerRemedyrepack Inc.
Strength75 mg / 1
Dosage FormTablet
Drug TypeOral
Package Quantity90 Tablet, Extended Release
Package Description90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-4065-0)
Active IngredientsVenlafaxine Hydrochloride
Marketing CategoryANDA

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NDC snapshot

Venlafaxine 75 mg / 1 Tablet is tracked under NDC 70518-4065-00 and rolls up into product family 70518-4065. Use this page to review package-level identifiers before comparing related family pages or starting a quote review.

  • Package configuration: 90 Tablet, Extended Release.
  • Manufacturer: Remedyrepack Inc..
  • Dosage form: Tablet.
  • Family size: 1 indexed presentation.

Official references

Use official labeling and directory references to confirm presentation details while your team reviews the PRN catalog entry and related sourcing paths.

Potential alternatives with matching presentation

Open the comparison hub or review package-level listings from 10 product-NDC families with matching normalized presentation details. Review each product detail page before treating any item as a true alternative.

View Potential Alternative Hubvenlafaxine 75 mg / 1 Tablet extended release 90 Tablet, Extended Release Bottle10 package-level listings in the comparison hub.

Sample package-level pages in this comparison set

Venlafaxine Hydrochloride - Venlafaxine 75 mg / 1 Tablet 90 Tablet, Extended Release, NDC 70518-4065-00, is a Remedyrepack Inc. 75 mg / 1 tablet presentation packaged as 90 Tablet, Extended Release.

NDC search formats

  • Canonical NDC 11: 70518-4065-00
  • Digits-only NDC 11: 70518406500
  • Possible 10-digit display format: 70518-4065-0 (7051840650)

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