Ofloxacin

Product NDC
55111-162
11-digit product format
551110162
Labeler code
55111
Product ID
55111-162_889d4bcc-0b25-f208-dea4-aedf75197224
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
ofloxacin
Dosage form
TABLET, COATED
Route
ORAL
Labeler
Dr. Reddy's Laboratories Limited
Application
ANDA077098
Marketing category
ANDA
Marketing start
2006-02-10
Marketing end
0000-00-00
Substance
OFLOXACIN
Active strength
400 mg/1
Pharmacologic classes
Quinolone Antimicrobial [EPC],Quinolones [CS]
NDC exclude flag
No
Listing certified through
2020-12-31
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
55111-162-01EA - Each55111-162e29fa706-a538-4d1b-b0d5-49416935769f12012-07-24

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
55111-162-0155111016201100 TABLET, COATED in 1 BOTTLE (55111-162-01) 2006-02-100000-00-00NoNoCurrent
55111-162-0555111016205500 TABLET, COATED in 1 BOTTLE (55111-162-05) 2006-02-100000-00-00NoNoCurrent
55111-162-305511101623030 TABLET, COATED in 1 BOTTLE (55111-162-30) 2006-02-100000-00-00NoNoCurrent
55111-162-505511101625050 TABLET, COATED in 1 BOTTLE (55111-162-50) 2006-02-100000-00-00NoNoCurrent
55111-162-785511101627810 BLISTER PACK in 1 CARTON (55111-162-78) > 10 TABLET, COATED in 1 BLISTER PACK (55111-162-79) 10 blister pack2006-02-100000-00-00NoNoCurrent