Label: DEX-MOXI PF- dexamethasone - moxifloxacin pf injection, solution
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Contains inactivated NDC Code(s)
NDC Code(s): 70261-512-01 - Packager: ImprimisRx NJ
- Category: HUMAN PRESCRIPTION DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
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Drug Label Information
Updated May 8, 2018
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INGREDIENTS AND APPEARANCE
DEX-MOXI PF
dexamethasone - moxifloxacin pf injection, solutionProduct Information Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:70261-512 Route of Administration INTRAOCULAR Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength DEXAMETHASONE SODIUM PHOSPHATE (UNII: AI9376Y64P) (DEXAMETHASONE - UNII:7S5I7G3JQL) DEXAMETHASONE PHOSPHATE 1 mg in 1 mL MOXIFLOXACIN HYDROCHLORIDE MONOHYDRATE (UNII: B8956S8609) (MOXIFLOXACIN - UNII:U188XYD42P) MOXIFLOXACIN 5 mg in 1 mL Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:70261-512-01 1 mL in 1 VIAL, SINGLE-USE; 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)