Ciprofloxacin

Product NDC

50090-3184

11-digit product format

500903184

Labeler code

50090

Product ID

50090-3184_818ac933-6d45-4b7a-9a6e-3f671646f132

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Ciprofloxacin Hydrochloride

Dosage form

SOLUTION/ DROPS

Route

OPHTHALMIC

Labeler

A-S Medication Solutions

Application

ANDA076555

Marketing category

ANDA

Marketing start

2009-07-24

Marketing end

0000-00-00

Substance

CIPROFLOXACIN HYDROCHLORIDE

Active strength

3 mg/mL

Pharmacologic classes

Quinolone Antimicrobial [EPC],Quinolones [CS]

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record