Oxybutynin 5 mg / 1 Tablet 30 Tablet, Film Coated, Extended Release

Reference details for licensed healthcare facility review and verification.

NDC 1100615-8219-39
Product NDC00615-8219
Generic Drug Nameoxybutynin
Brand Nameoxybutynin
ManufacturerNCS HealthCare of KY, LLC dba Vangard Labs
Strength5 mg / 1
Dosage FormTablet
Drug TypeOral
Package Quantity30 Tablet, Film Coated, Extended Release
Package Description30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (0615-8219-39)
Active IngredientsOxybutynin Chloride
Marketing CategoryANDA

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NDC snapshot

oxybutynin 5 mg / 1 Tablet is tracked under NDC 00615-8219-39 and rolls up into product family 00615-8219. 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: NCS HealthCare of KY, LLC dba Vangard Labs.
  • 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.

Oxybutynin 5 mg / 1 Tablet 30 Tablet, Film Coated, Extended Release, NDC 00615-8219-39, is a NCS HealthCare of KY, LLC dba Vangard Labs 5 mg / 1 tablet presentation packaged as 30 Tablet, Film Coated, Extended Release.

NDC search formats

  • Canonical NDC 11: 00615-8219-39
  • Digits-only NDC 11: 00615821939
  • Possible 10-digit display format: 0615-8219-39 (0615821939)

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