Ciprofloxacin Hydrochloride 500 mg / 1 Tablet 1 Tablet, Film Coated

Reference details for licensed healthcare facility review and verification.

NDC 1183939-0002-01
Product NDC83939-0002
Generic Drug NameCiprofloxacin Hydrochloride
Brand NameCiprofloxacin Hydrochloride
ManufacturerVerityrx, Llc
Strength500 mg / 1
Dosage FormTablet
Drug TypeOral
Package Quantity1 Tablet, Film Coated
Package Description1 TABLET, FILM COATED in 1 POUCH (83939-0002-1)
Active IngredientsCiprofloxacin Hydrochloride
Marketing CategoryANDA

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NDC snapshot

Ciprofloxacin Hydrochloride 500 mg / 1 Tablet is tracked under NDC 83939-0002-01 and rolls up into product family 83939-0002. Use this page to review package-level identifiers before comparing related family pages or starting a quote review.

  • Package configuration: 1 Tablet, Film Coated.
  • Manufacturer: Verityrx, Llc.
  • 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.

Ciprofloxacin Hydrochloride 500 mg / 1 Tablet 1 Tablet, Film Coated, NDC 83939-0002-01, is a Verityrx, Llc 500 mg / 1 tablet presentation packaged as 1 Tablet, Film Coated.

NDC search formats

  • Canonical NDC 11: 83939-0002-01
  • Digits-only NDC 11: 83939000201
  • Possible 10-digit display format: 83939-0002-1 (8393900021)

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