Ciprofloxacin Hydrochloride

Product NDC
55700-636
11-digit product format
557000636
Labeler code
55700
Product ID
55700-636_b56a55d9-29fd-497e-b2d9-276a70204f31
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Ciprofloxacin Hydrochloride
Dosage form
SOLUTION/ DROPS
Route
OPHTHALMIC
Labeler
Lake Erie Medical DBA Quality Care Products LLC
Application
NDA019992
Marketing category
NDA AUTHORIZED GENERIC
Marketing start
2018-06-08
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
55700-636-052021-04-14C16284748780-1ba0f9c33-24b5-a910-e053-dadaa90a0b8505af8e0e-4e3e-4299-bb38-382f930fc1eb
55700-636-052021-01-29C16284748780-1ba0f9c33-24b5-a910-e053-dadaa90a0b8505af8e0e-4e3e-4299-bb38-382f930fc1eb