Terbinafine Hydrochloride 250 mg / 1 Tablet 500 Tablet

Reference details for licensed healthcare facility review and verification.

NDC 1155111-0250-05
Product NDC55111-0250
Generic Drug NameTerbinafine Hydrochloride
Brand NameTerbinafine Hydrochloride
ManufacturerDr.Reddys Laboratories Limited
Strength250 mg / 1
Dosage FormTablet
Drug TypeOral
Package Quantity500 Tablet
Package Description500 TABLET in 1 BOTTLE (55111-250-05)
Active IngredientsTerbinafine Hydrochloride
Marketing CategoryANDA

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NDC snapshot

Terbinafine Hydrochloride 250 mg / 1 Tablet is tracked under NDC 55111-0250-05 and rolls up into product family 55111-0250. Use this page to review package-level identifiers before comparing related family pages or starting a quote review.

  • Package configuration: 500 Tablet.
  • Manufacturer: Dr.Reddys Laboratories Limited.
  • Dosage form: Tablet.
  • Family size: 5 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.

Terbinafine Hydrochloride 250 mg / 1 Tablet 500 Tablet, NDC 55111-0250-05, is a Dr.Reddys Laboratories Limited 250 mg / 1 tablet presentation packaged as 500 Tablet.

NDC search formats

  • Canonical NDC 11: 55111-0250-05
  • Digits-only NDC 11: 55111025005
  • Possible 10-digit display formats: 55111-250-05 (5511125005), 55111-0250-5 (5511102505)

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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