Tiagabine Hydrochloride 4 mg / 1 Tablet 100 Tablet, Film Coated

Reference details for licensed healthcare facility review and verification.

NDC 1162756-0224-08
Product NDC62756-0224
Generic Drug NameTiagabine Hydrochloride
Brand NameTiagabine Hydrochloride
ManufacturerSun Pharmaceutical Industries, Inc.
Strength4 mg / 1
Dosage FormTablet
Drug TypeOral
Package Quantity100 Tablet, Film Coated
Package Description100 TABLET, FILM COATED in 1 BOTTLE (62756-224-08)
Active IngredientsTiagabine Hydrochloride
Marketing CategoryANDA

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NDC snapshot

Tiagabine Hydrochloride 4 mg / 1 Tablet is tracked under NDC 62756-0224-08 and rolls up into product family 62756-0224. Use this page to review package-level identifiers before comparing related family pages or starting a quote review.

  • Package configuration: 100 Tablet, Film Coated.
  • Manufacturer: Sun Pharmaceutical Industries, Inc..
  • Dosage form: Tablet.
  • Family size: 4 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.

Tiagabine Hydrochloride 4 mg / 1 Tablet 100 Tablet, Film Coated, NDC 62756-0224-08, is a Sun Pharmaceutical Industries, Inc. 4 mg / 1 tablet presentation packaged as 100 Tablet, Film Coated.

NDC search formats

  • Canonical NDC 11: 62756-0224-08
  • Digits-only NDC 11: 62756022408
  • Possible 10-digit display formats: 62756-224-08 (6275622408), 62756-0224-8 (6275602248)

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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