Quetiapine, Extended Release 150 mg / 1 Tablet 30 Tablet, Film Coated, Extended Release

Reference details for licensed healthcare facility review and verification.

NDC 1170518-4051-00
Product NDC70518-4051
Generic Drug NameQuetiapine, Extended Release
Brand NameQuetiapine, Extended Release
ManufacturerRemedyrepack Inc.
Strength150 mg / 1
Dosage FormTablet
Drug TypeOral
Package Quantity30 Tablet, Film Coated, Extended Release
Package Description30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (70518-4051-0)
Active IngredientsQuetiapine Fumarate
Marketing CategoryANDA

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NDC snapshot

Quetiapine, Extended Release 150 mg / 1 Tablet is tracked under NDC 70518-4051-00 and rolls up into product family 70518-4051. Use this page to review package-level identifiers before comparing related family pages or starting a quote review.

  • Package configuration: 30 Tablet, Film Coated, 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.

Quetiapine, Extended Release 150 mg / 1 Tablet 30 Tablet, Film Coated, Extended Release, NDC 70518-4051-00, is a Remedyrepack Inc. 150 mg / 1 tablet presentation packaged as 30 Tablet, Film Coated, Extended Release.

NDC search formats

  • Canonical NDC 11: 70518-4051-00
  • Digits-only NDC 11: 70518405100
  • Possible 10-digit display format: 70518-4051-0 (7051840510)

Helpful product links

  • Search by brand name: Quetiapine, Extended Release
  • NDC 11: 70518-4051-00
  • Product family NDC: 70518-4051
  • VA classification code: CN709
  • VA classification code description: ANTIPSYCHOTICS,OTHER
  • CMOP ID: Q0049
  • VUID: 4028300