Darifenacin - Hydrobromide 7.5 mg / 1 Tablet 30 Tablet, Extended Release

Reference details for licensed healthcare facility review and verification.

NDC 1169097-0431-02
Product NDC69097-0431
Generic Drug NameDarifenacin Hydrobromide
Brand NameDarifenacin
ManufacturerCipla USA Inc.
Strength7.5 mg / 1
Dosage FormTablet
Drug TypeOral
Package Quantity30 Tablet, Extended Release
Package Description30 TABLET, EXTENDED RELEASE in 1 BOTTLE (69097-431-02)
Active IngredientsDarifenacin Hydrobromide
Marketing CategoryANDA

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NDC snapshot

Darifenacin Hydrobromide 7.5 mg / 1 Tablet is tracked under NDC 69097-0431-02 and rolls up into product family 69097-0431. Use this page to review package-level identifiers before comparing related family pages or starting a quote review.

  • Package configuration: 30 Tablet, Extended Release.
  • Manufacturer: Cipla USA 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.

Darifenacin - Hydrobromide 7.5 mg / 1 Tablet 30 Tablet, Extended Release, NDC 69097-0431-02, is a Cipla USA Inc. 7.5 mg / 1 tablet presentation packaged as 30 Tablet, Extended Release.

NDC search formats

  • Canonical NDC 11: 69097-0431-02
  • Digits-only NDC 11: 69097043102
  • Possible 10-digit display formats: 69097-431-02 (6909743102), 69097-0431-2 (6909704312)

Multiple 10-digit display-format aliases can map to the same stored 11-digit billing NDC, so these are shown as search aliases rather than a single asserted package format.

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