10370-108 : Ciprofloxacin Oral Tablet, Film Coated, Extended Release


NDC10370-108
Labeler: Par Pharmaceutical, Inc.
Product Type: Human Prescription Drug
Drug Name:  Ciprofloxacin Extended-release
Dosage Form: Oral Tablet, Film Coated, Extended Release
Application #: ANDA078166
Rev. Date: 


Appearance:


Markings: ANCHEN;108
Shapes:  Oval
Colors:  White
Size (mm): 19
Segments: * 1

* Segments = the number of equally sized pieces which the pill can be broken into. In this case, a value of 1 indicates a solid pill with no score lines.

NDC Package Codes:

  • 10370-108-05: 50 TABLET, FILM COATED, EXTENDED RELEASE IN 1 BOTTLE (10370‑108‑05)
  • 10370-108-10: 100 TABLET, FILM COATED, EXTENDED RELEASE IN 1 BOTTLE (10370‑108‑10)

Active Ingredients:

  • Ciprofloxacin
  • Ciprofloxacin Hydrochloride

Dosage Strength:

  • 574.9 mg
  • 425.2 mg

Inactive Ingredients:

  • Triacetin
  • Silicon Dioxide
  • Crospovidone
  • D&c Yellow No. 10
  • Hydrogenated Cottonseed Oil
  • Hypromelloses
  • Maltodextrin
  • Cellulose, Microcrystalline
  • Polydextrose
  • Polyethylene Glycols
  • Titanium Dioxide
  • Succinic Acid
  • Lactitol
  • Magnesium Stearate

Pharmaceutical Classes:

  • Quinolone Antimicrobial [EPC]
  • Quinolones [Chemical/Ingredient]

Related Products:

Based on records with the same trade name.
  • 10370-107 Ciprofloxacin Oral Tablet, Film Coated, Extended Release by Par Pharmaceutical, Inc.

NDC QR Code

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