Ciprofloxacin Hydrochloride 61314-0656-10

Package NDC

61314-0656-10

Manufacturer: Sandoz Inc
Dosage Form: Solution/ Drops
Route: Ophthalmic
Product Type: Human Prescription Drug
Marketing Start: May 7, 2004
Listing Expires: December 31, 2026
Application: NDA019992

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Active Ingredients

Ingredient	Strength
Ciprofloxacin Hydrochloride	3 mg/mL

Drug Class

Quinolone Antimicrobial [EPC]Quinolones [CS]

Selected Package

61314-0656-10Selected

1 BOTTLE, PLASTIC in 1 CARTON (61314-656-10) / 10 mL in 1 BOTTLE, PLASTIC

Other packages for this product(2)

61314-0656-05

1 BOTTLE, PLASTIC in 1 CARTON (61314-656-05) / 5 mL in 1 BOTTLE, PLASTIC

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61314-0656-25

1 BOTTLE, PLASTIC in 1 CARTON (61314-656-25) / 2.5 mL in 1 BOTTLE, PLASTIC

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