Moxifloxacin

Product NDC
55700-657
11-digit product format
557000657
Labeler code
55700
Product ID
55700-657_2468dc10-eb71-49b4-a857-31448c6c4bb8
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Moxifloxacin
Dosage form
SOLUTION/ DROPS
Route
OPHTHALMIC
Labeler
Lake Erie Medical DBA Quality Care Products LLC
Application
ANDA202916
Marketing category
ANDA
Marketing start
2018-07-20
Marketing end
0000-00-00
Substance
MOXIFLOXACIN HYDROCHLORIDE
Active strength
5 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

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
55700-657-03ML - Milliliter55700-65779189bb0-66f4-4a19-bf43-f16041a4057912018-08-13