Quetiapine, Extended Release 200 mg / 1 Tablet 1000 Tablet, Film Coated, Extended Release

Reference details for licensed healthcare facility review and verification.

NDC 1150228-0382-10
Product NDC50228-0382
Generic Drug NameQuetiapine, Extended Release
Brand NameQuetiapine, Extended Release
ManufacturerScieGen Pharmaceuticals, Inc
Strength200 mg / 1
Dosage FormTablet
Drug TypeOral
Package Quantity1000 Tablet, Film Coated, Extended Release
Package Description1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50228-382-10)
Active IngredientsQuetiapine Fumarate
Marketing CategoryANDA

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NDC snapshot

Quetiapine, Extended Release 200 mg / 1 Tablet is tracked under NDC 50228-0382-10 and rolls up into product family 50228-0382. Use this page to review package-level identifiers before comparing related family pages or starting a quote review.

  • Package configuration: 1000 Tablet, Film Coated, Extended Release.
  • Manufacturer: ScieGen Pharmaceuticals, 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

These nearby package-level pages can help healthcare teams compare related packaging or presentation differences inside the same product-NDC family.

Quetiapine, Extended Release 200 mg / 1 Tablet 1000 Tablet, Film Coated, Extended Release, NDC 50228-0382-10, is a ScieGen Pharmaceuticals, Inc 200 mg / 1 tablet presentation packaged as 1000 Tablet, Film Coated, Extended Release.

NDC search formats

  • Canonical NDC 11: 50228-0382-10
  • Digits-only NDC 11: 50228038210
  • Possible 10-digit display format: 50228-382-10 (5022838210)

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