Fluoxetine Hydrochloride 10 mg / 1 Tablet 100 Tablet, Film Coated

Reference details for licensed healthcare facility review and verification.

NDC 1146708-0242-31
Product NDC46708-0242
Generic Drug NameFluoxetine Hydrochloride
Brand NameFluoxetine Hydrochloride
ManufacturerAlembic Pharmaceuticals Limited
Strength10 mg / 1
Dosage FormTablet
Drug TypeOral
Package Quantity100 Tablet, Film Coated
Package Description100 TABLET, FILM COATED in 1 BOTTLE (46708-242-31)
Active IngredientsFluoxetine Hydrochloride
Marketing CategoryANDA

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NDC snapshot

Fluoxetine Hydrochloride 10 mg / 1 Tablet is tracked under NDC 46708-0242-31 and rolls up into product family 46708-0242. 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: Alembic Pharmaceuticals Limited.
  • 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.

Fluoxetine Hydrochloride 10 mg / 1 Tablet 100 Tablet, Film Coated, NDC 46708-0242-31, is a Alembic Pharmaceuticals Limited 10 mg / 1 tablet presentation packaged as 100 Tablet, Film Coated.

NDC search formats

  • Canonical NDC 11: 46708-0242-31
  • Digits-only NDC 11: 46708024231
  • Possible 10-digit display format: 46708-242-31 (4670824231)

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