10370-108 : Ciprofloxacin Oral Tablet, Film Coated, Extended Release
NDC: | 10370-108 |
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
Scan the QR code below to easily reference this data in the future:< Prev: 10370-107Next: 10370-116 >
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Note: The RxChat NDC Database uses publicly available data from the FDA and the U.S. National Library of Medicine (NLM); The NLM is not responsible for the data presented and does not endorse or recommend this or any other product. While we make every effort to ensure that the information presented is accurate, you should assume that all results are unvalidated. To report any errors or inconsistencies please contact us.