13913-001 : 24 Hr Proquin 500 mg Extended Release Tablet
NDC: | 13913-001 |
Labeler: | Depomed, Inc. |
Product Type: | Human Prescription Drug |
Drug Name: | Proquin XR |
Dosage Form: | Oral Tablet, Film Coated, Extended Release |
Application #: | NDA021744 |
Rev. Date: |
Appearance:
Markings: | DMI;500 |
Shapes: |
Oval |
Colors: |
Blue |
Size (mm): | 18 |
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:
- 13913-001-03: 1 BLISTER PACK IN 1 CARTON (13913‑001‑03) > 3 TABLET, FILM COATED, EXTENDED RELEASE IN 1 BLISTER PACK
- 13913-001-30: 30 TABLET, FILM COATED, EXTENDED RELEASE IN 1 BOTTLE (13913‑001‑30)
- 13913-001-91: 1 BLISTER PACK IN 1 CARTON (13913‑001‑91) > 1 TABLET, FILM COATED, EXTENDED RELEASE IN 1 BLISTER PACK
Active Ingredients:
- Ciprofloxacin Hydrochloride
Dosage Strength:
- 500 mg
Inactive Ingredients:
- Povidone
- Magnesium Stearate
- Polyethylene Glycol
Pharmaceutical Classes:
- Quinolone Antimicrobial [EPC]
- Quinolones [CS]
NDC QR Code
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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.