Label: SODIUM CHLORIDE injection, solution
- NDC Code(s): 85036-500-01, 85036-500-02
- Packager: Vin TRADING LLC
- Category: HUMAN PRESCRIPTION DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
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Drug Label Information
Updated December 13, 2024
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INGREDIENTS AND APPEARANCE
SODIUM CHLORIDE
sodium chloride injection, solutionProduct Information Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:85036-500 Route of Administration INTRAVENOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SODIUM CHLORIDE (UNII: 451W47IQ8X) (CHLORIDE ION - UNII:Q32ZN48698) SODIUM CHLORIDE 4.5 g in 500 mL Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:85036-500-02 30 in 1 CARTON 12/11/2024 1 NDC:85036-500-01 500 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 12/11/2024 Labeler - Vin TRADING LLC (120880762)