Ciprofloxacin

Product NDC
55700-245
11-digit product format
557000245
Labeler code
55700
Product ID
55700-245_15bd7469-0b0f-4479-a86e-dad3b7694ec6
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Ciprofloxacin Hydrochloride
Dosage form
SOLUTION/ DROPS
Route
OPHTHALMIC
Labeler
Lake Erie Medical DBA Quality Care Products LLC
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
2020-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
55700-245-052025-01-08C16284748780-1ba0f9c33-3696-a910-e053-dadaa90a0b855a4327fb-9517-46d6-8d54-a5f2c1520442
55700-245-052021-01-29C16284748780-1ba0f9c33-3696-a910-e053-dadaa90a0b855a4327fb-9517-46d6-8d54-a5f2c1520442

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
55700-245-05ML - Milliliter55700-24514f30e6f-28f9-4904-a463-7a3f55e3796c12016-12-07