Ciprofloxacin

Product NDC
68071-2391
11-digit product format
680712391
Labeler code
68071
Product ID
68071-2391_c0a7985c-0aeb-29f3-e053-2a95a90aad50
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Ciprofloxacin
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
NuCare Pharmaceuticals,Inc.
Application
ANDA075593
Marketing category
ANDA
Marketing start
2004-06-09
Marketing end
0000-00-00
Substance
CIPROFLOXACIN HYDROCHLORIDE
Active strength
500 mg/1
Pharmacologic classes
Quinolone Antimicrobial [EPC],Quinolones [CS]
NDC exclude flag
No
Listing certified through
2022-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
68071-2391CIPROFLOXACIN TABLET, FILM COATED [NUCARE PHARMACEUTICALS,INC.]1Legacy NDC20210424_c0a7c783-8c8e-e0fc-e053-2a95a90a9548.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
68071-2391-16807123910110 TABLET, FILM COATED in 1 BOTTLE (68071-2391-1) 2021-04-230000-00-00NoNoCurrent
68071-2391-26807123910220 TABLET, FILM COATED in 1 BOTTLE (68071-2391-2) 2021-04-230000-00-00NoNoCurrent
68071-2391-36807123910330 TABLET, FILM COATED in 1 BOTTLE (68071-2391-3) 2021-04-230000-00-00NoNoCurrent
68071-2391-46807123910414 TABLET, FILM COATED in 1 BOTTLE (68071-2391-4) 2021-04-230000-00-00NoNoCurrent
68071-2391-66807123910660 TABLET, FILM COATED in 1 BOTTLE (68071-2391-6) 2021-04-230000-00-00NoNoCurrent
68071-2391-76807123910721 TABLET, FILM COATED in 1 BOTTLE (68071-2391-7) 2021-04-230000-00-00NoNoCurrent
68071-2391-86807123910828 TABLET, FILM COATED in 1 BOTTLE (68071-2391-8) 2021-04-230000-00-00NoNoCurrent