Deflazacort 36 mg / 1 Tablet 1 Bottle

Reference details for licensed healthcare facility review and verification.

NDC 1170095-0043-30
Product NDC70095-0043
Generic Drug NameDeflazacort
Brand NameDeflazacort
ManufacturerSun Pharmaceutical Industries, Inc.
Strength36 mg / 1
Dosage FormTablet
Drug TypeOral
Package Quantity1 Bottle
Package Description1 BOTTLE in 1 CARTON (70095-043-30) / 30 TABLET in 1 BOTTLE
Active IngredientsDeflazacort
Marketing CategoryANDA

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NDC snapshot

Deflazacort 36 mg / 1 Tablet is tracked under NDC 70095-0043-30 and rolls up into product family 70095-0043. Use this page to review package-level identifiers before comparing related family pages or starting a quote review.

  • Package configuration: 1 Bottle.
  • Manufacturer: Sun Pharmaceutical Industries, Inc..
  • Dosage form: Tablet.
  • Family size: 1 indexed presentation.

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Official references

Use official labeling and directory references to confirm presentation details while your team reviews the PRN catalog entry and related sourcing paths.

Potential alternatives with matching presentation

Open the comparison hub or review package-level listings from 7 product-NDC families with matching normalized presentation details. Review each product detail page before treating any item as a true alternative.

View Potential Alternative Hubdeflazacort 36 mg / 1 Tablet 1 Bottle Bottle7 package-level listings in the comparison hub.

Sample package-level pages in this comparison set

Deflazacort 36 mg / 1 Tablet 1 Bottle, NDC 70095-0043-30, is a Sun Pharmaceutical Industries, Inc. 36 mg / 1 tablet presentation packaged as 1 Bottle.

NDC search formats

  • Canonical NDC 11: 70095-0043-30
  • Digits-only NDC 11: 70095004330
  • Possible 10-digit display format: 70095-043-30 (7009504330)

Helpful product links

  • Search by brand name: Deflazacort
  • NDC 11: 70095-0043-30
  • Product family NDC: 70095-0043
  • VA classification code: HS051
  • VA classification code description: GLUCOCORTICOIDS
  • CMOP ID: D1145
  • VUID: 4036434