Label: PROMETHAZINE HCL injection, solution
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Contains inactivated NDC Code(s)
NDC Code(s): 52533-204-12 - Packager: Cantrell Drug Company
- Category: HUMAN PRESCRIPTION DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
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Drug Label Information
Updated May 27, 2014
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INGREDIENTS AND APPEARANCE
PROMETHAZINE HCL
promethazine hcl injection, solutionProduct Information Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:52533-204 Route of Administration INTRAVENOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength PROMETHAZINE HYDROCHLORIDE (UNII: R61ZEH7I1I) (PROMETHAZINE - UNII:FF28EJQ494) PROMETHAZINE HYDROCHLORIDE 0.625 mg in 1 mL Inactive Ingredients Ingredient Name Strength SODIUM CHLORIDE (UNII: 451W47IQ8X) 9 mg in 1 mL EDETATE SODIUM (UNII: MP1J8420LU) 0.013 mg in 1 mL CALCIUM CHLORIDE (UNII: M4I0D6VV5M) 0.005 mg in 1 mL SODIUM METABISULFITE (UNII: 4VON5FNS3C) 0.03 mg in 1 mL PHENOL (UNII: 339NCG44TV) 0.6375 mg in 1 mL WATER (UNII: 059QF0KO0R) Other Ingredients Ingredient Kind Ingredient Name Quantity May contain ACETIC ACID (UNII: Q40Q9N063P) May contain SODIUM ACETATE (UNII: 4550K0SC9B) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:52533-204-12 10 mL in 1 SYRINGE, PLASTIC Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 05/27/2014 Labeler - Cantrell Drug Company (035545763)