Venlafaxine 150 mg / 1 Tablet 30 Tablet, Extended Release

Reference details for licensed healthcare facility review and verification.

NDC 1170710-1350-03
Product NDC70710-1350
Generic Drug NameVenlafaxine
Brand NameVenlafaxine
ManufacturerZydus Pharmaceuticals USA Inc.
Strength150 mg / 1
Dosage FormTablet
Drug TypeOral
Package Quantity30 Tablet, Extended Release
Package Description30 TABLET, EXTENDED RELEASE in 1 BOTTLE (70710-1350-3)
Active IngredientsVenlafaxine Hydrochloride
Marketing CategoryANDA

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NDC snapshot

Venlafaxine 150 mg / 1 Tablet is tracked under NDC 70710-1350-03 and rolls up into product family 70710-1350. Use this page to review package-level identifiers before comparing related family pages or starting a quote review.

  • Package configuration: 30 Tablet, Extended Release.
  • Manufacturer: Zydus Pharmaceuticals USA Inc..
  • Dosage form: Tablet.
  • Family size: 3 indexed presentations.

Official references

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

Alternate presentations in this family

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Potential alternatives with matching presentation

Open the comparison hub or review package-level listings from 9 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 150 mg / 1 Tablet extended release 30 Tablet, Extended Release Bottle9 package-level listings in the comparison hub.

Sample package-level pages in this comparison set

Venlafaxine 150 mg / 1 Tablet 30 Tablet, Extended Release, NDC 70710-1350-03, is a Zydus Pharmaceuticals USA Inc. 150 mg / 1 tablet presentation packaged as 30 Tablet, Extended Release.

NDC search formats

  • Canonical NDC 11: 70710-1350-03
  • Digits-only NDC 11: 70710135003
  • Possible 10-digit display format: 70710-1350-3 (7071013503)

Helpful product links