Bupropion hydrochloride, (Xl) 150 mg / 1 Tablet 500 Tablet, Extended Release

Reference details for licensed healthcare facility review and verification.

NDC 1124979-0101-02
Product NDC24979-0101
Generic Drug Namebupropion hydrochloride, (Xl)
Brand NameBupropion Hydrochloride, (Xl)
ManufacturerTWi Pharmaceuticals, Inc.
Strength150 mg / 1
Dosage FormTablet
Drug TypeOral
Package Quantity500 Tablet, Extended Release
Package Description500 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (24979-101-02)
Active IngredientsBupropion Hydrochloride
Marketing CategoryANDA

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NDC snapshot

bupropion hydrochloride, (Xl) 150 mg / 1 Tablet is tracked under NDC 24979-0101-02 and rolls up into product family 24979-0101. Use this page to review package-level identifiers before comparing related family pages or starting a quote review.

  • Package configuration: 500 Tablet, Extended Release.
  • Manufacturer: TWi Pharmaceuticals, Inc..
  • Dosage form: Tablet.
  • Family size: 3 indexed presentations.

Official references

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Alternate presentations in this family

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Potential alternatives with matching presentation

Open the comparison hub or review package-level listings from 12 product-NDC families with matching normalized presentation details. Review each product detail page before treating any item as a true alternative.

View Potential Alternative Hubbupropion hydrochloride, (Xl) 150 mg / 1 Tablet extended release 500 Tablet, Extended Release Bottle12 package-level listings in the comparison hub.

Sample package-level pages in this comparison set

Bupropion hydrochloride, (Xl) 150 mg / 1 Tablet 500 Tablet, Extended Release, NDC 24979-0101-02, is a TWi Pharmaceuticals, Inc. 150 mg / 1 tablet presentation packaged as 500 Tablet, Extended Release.

NDC search formats

  • Canonical NDC 11: 24979-0101-02
  • Digits-only NDC 11: 24979010102
  • Possible 10-digit display format: 24979-101-02 (2497910102)

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