Avelox

Product NDC
0085-1737
11-digit product format
000851737
Labeler code
0085
Product ID
0085-1737_9ae0561c-5e62-425f-a7f3-5cdbb842de80
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
moxifloxacin hydrochloride
Dosage form
INJECTION, SOLUTION
Route
INTRAVENOUS
Labeler
Schering Plough Corporation
Application
NDA021277
Marketing category
NDA
Marketing start
2001-11-30
Marketing end
0000-00-00
Substance
MOXIFLOXACIN HYDROCHLORIDE
Active strength
400 mg/250mL
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
0085-1737-01ML - Milliliter0085-1737884a4624-bd01-44f7-894e-1760cce874f312012-07-24