Ofloxacin

Product NDC
55111-160
11-digit product format
551110160
Labeler code
55111
Product ID
55111-160_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
200 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
55111-160-50EA - Each55111-16013cdac75-d166-43d4-b6fe-a384078bf10212012-07-24

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
55111-160-0155111016001100 TABLET, COATED in 1 BOTTLE (55111-160-01) 2006-02-100000-00-00NoNoCurrent
55111-160-0555111016005500 TABLET, COATED in 1 BOTTLE (55111-160-05) 2006-02-100000-00-00NoNoCurrent
55111-160-305511101603030 TABLET, COATED in 1 BOTTLE (55111-160-30) 2006-02-100000-00-00NoNoCurrent
55111-160-505511101605050 TABLET, COATED in 1 BOTTLE (55111-160-50) 2006-02-100000-00-00NoNoCurrent
55111-160-785511101607810 BLISTER PACK in 1 CARTON (55111-160-78) > 10 TABLET, COATED in 1 BLISTER PACK (55111-160-79) 10 blister pack2006-02-100000-00-00NoNoCurrent