NDC 16714-643

MOXIFLOXACIN

Moxifloxacin

MOXIFLOXACIN is a Ophthalmic Solution/ Drops in the Human Prescription Drug category. It is labeled and distributed by Northstar Rx Llc. The primary component is Moxifloxacin Hydrochloride.

Product ID16714-643_c11c970c-ffa6-4661-b515-708bae4eddd6
NDC16714-643
Product TypeHuman Prescription Drug
Proprietary NameMOXIFLOXACIN
Generic NameMoxifloxacin
Dosage FormSolution/ Drops
Route of AdministrationOPHTHALMIC
Marketing Start Date2017-10-04
Marketing CategoryANDA /
Application NumberANDA206242
Labeler NameNorthStar Rx LLC
Substance NameMOXIFLOXACIN HYDROCHLORIDE
Active Ingredient Strength5 mg/mL
Pharm ClassesQuinolone Antimicrobial [EPC], Quinolones [CS]
NDC Exclude FlagN
Listing Certified Through2023-12-31

Packaging

NDC 16714-643-01

1 BOTTLE in 1 CARTON (16714-643-01) > 3 mL in 1 BOTTLE
Marketing Start Date2017-10-04
NDC Exclude FlagN
Sample Package?N

Drug Details

NDC Crossover Matching brand name "MOXIFLOXACIN" or generic name "Moxifloxacin"

NDCBrand NameGeneric Name
0378-5430Moxifloxacinmoxifloxacin
0904-6406MoxifloxacinMoxifloxacin
16714-643MOXIFLOXACINMOXIFLOXACIN
17478-519MoxifloxacinMoxifloxacin
48792-7823Moxifloxacinmoxifloxacin hydrochloride
50090-3091Moxifloxacinmoxifloxacin
50090-3147MoxifloxacinMoxifloxacin
50090-5279MoxifloxacinMoxifloxacin
53217-347Moxifloxacinmoxifloxacin
55111-112MoxifloxacinMoxifloxacin
55700-638MoxifloxacinMoxifloxacin
55700-657MoxifloxacinMoxifloxacin
60505-0582Moxifloxacinmoxifloxacin
61919-553MOXIFLOXACINMOXIFLOXACIN
63323-850MoxifloxacinMOXIFLOXACIN HYDROCHLORIDE
63629-8357MoxifloxacinMoxifloxacin
65862-840MOXIFLOXACINMOXIFLOXACIN
66298-8507MoxifloxacinMOXIFLOXACIN HYDROCHLORIDE
67296-1679MoxifloxacinMoxifloxacin
68180-421MOXIFLOXACINMOXIFLOXACIN
68180-422MoxifloxacinMoxifloxacin
68788-7404Moxifloxacinmoxifloxacin
72189-076MOXIFLOXACINMOXIFLOXACIN
© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.