63304-709 : Ciprofloxacin 250 mg (As Ciprofloxacin Hydrochloride 297 mg) Oral Tablet

NDC:	63304-709
Labeler:	Ranbaxy Pharmaceuticals Inc.
Product Type:	Human Prescription Drug
Drug Name:	Ciprofloxacin
Dosage Form:	Oral Tablet, Film Coated
Application #:	ANDA075747
Rev. Date:	Jun 9, 2004

Appearance:

Markings:	RX709
Shapes:	Round
Colors:	White
Size (mm):	10
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:

63304-709-01: 100 TABLET, FILM COATED IN 1 BOTTLE (63304‑709‑01)
63304-709-05: 500 TABLET, FILM COATED IN 1 BOTTLE (63304‑709‑05)
63304-709-14: 14 TABLET, FILM COATED IN 1 BOTTLE (63304‑709‑14)
63304-709-80: 100 TABLET, FILM COATED IN 1 BLISTER PACK (63304‑709‑80)

Active Ingredients:

Ciprofloxacin Hydrochloride

Dosage Strength:

250 mg

Inactive Ingredients:

Silicon Dioxide
Starch, Corn
Hypromelloses
Magnesium Stearate
Cellulose, Microcrystalline
Polyethylene Glycols
Talc
Titanium Dioxide
Sodium Starch Glycolate Type a Potato

Pharmaceutical Classes:

Quinolone Antimicrobial [EPC]
Quinolones [CS]

NDC QR Code

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NDC 63304-709 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.