Oxybutynin 5 mg / 1 Tablet 60 Tablet, Film Coated, Extended Release

Reference details for licensed healthcare facility review and verification.

NDC 1168382-0255-14
Product NDC68382-0255
Generic Drug Nameoxybutynin
Brand Nameoxybutynin
ManufacturerZydus Pharmaceuticals USA Inc.
Strength5 mg / 1
Dosage FormTablet
Drug TypeOral
Package Quantity60 Tablet, Film Coated, Extended Release
Package Description60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68382-255-14)
Active IngredientsOxybutynin Chloride
Marketing CategoryANDA

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NDC snapshot

oxybutynin 5 mg / 1 Tablet is tracked under NDC 68382-0255-14 and rolls up into product family 68382-0255. Use this page to review package-level identifiers before comparing related family pages or starting a quote review.

  • Package configuration: 60 Tablet, Film Coated, Extended Release.
  • Manufacturer: Zydus Pharmaceuticals USA Inc..
  • Dosage form: Tablet.
  • Family size: 6 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 2 product-NDC families with matching normalized presentation details. Review each product detail page before treating any item as a true alternative.

View Potential Alternative Huboxybutynin 5 mg / 1 Tablet extended release 60 Tablet, Film Coated, Extended Release Bottle2 package-level listings in the comparison hub.

Sample package-level pages in this comparison set

Oxybutynin 5 mg / 1 Tablet 60 Tablet, Film Coated, Extended Release, NDC 68382-0255-14, is a Zydus Pharmaceuticals USA Inc. 5 mg / 1 tablet presentation packaged as 60 Tablet, Film Coated, Extended Release.

NDC search formats

  • Canonical NDC 11: 68382-0255-14
  • Digits-only NDC 11: 68382025514
  • Possible 10-digit display format: 68382-255-14 (6838225514)

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