Label: MOXIFLOXACIN PF injection, solution
- Category: HUMAN PRESCRIPTION DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
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Updated May 8, 2018
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- STORAGE AND HANDLING
- Vial Label
INGREDIENTS AND APPEARANCE
moxifloxacin pf injection, solution
Product Information Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:70261-511 Route of Administration INTRAOCULAR Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MOXIFLOXACIN HYDROCHLORIDE MONOHYDRATE (UNII: B8956S8609) (MOXIFLOXACIN - UNII:U188XYD42P) MOXIFLOXACIN 5 mg in 1 mL Inactive Ingredients Ingredient Name Strength SODIUM CHLORIDE (UNII: 451W47IQ8X) 8 mg in 1 mL Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:70261-511-01 1 mL in 1 VIAL, GLASS; Type 0: Not a Combination Product 01/01/2018 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 01/01/2018 Labeler - ImprimisRx NJ (931390178) Registrant - ImprimisRx NJ (931390178) Establishment Name Address ID/FEI Business Operations Imprimis Pharmaceuticals 080431967 manufacture(70261-511)