Label: DILTIAZEM HCL injection, solution
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Contains inactivated NDC Code(s)
NDC Code(s): 52533-198-76 - 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 January 12, 2015
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INGREDIENTS AND APPEARANCE
DILTIAZEM HCL
diltiazem hcl injection, solutionProduct Information Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:52533-198 Route of Administration INTRAVENOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength DILTIAZEM HYDROCHLORIDE (UNII: OLH94387TE) (DILTIAZEM - UNII:EE92BBP03H) DILTIAZEM HYDROCHLORIDE 0.83 mg in 1 mL Inactive Ingredients Ingredient Name Strength DEXTROSE (UNII: IY9XDZ35W2) 50 mg in 1 mL ANHYDROUS CITRIC ACID (UNII: XF417D3PSL) 0.125 mg in 1 mL TRISODIUM CITRATE DIHYDRATE (UNII: B22547B95K) 0.11 mg in 1 mL SORBITOL (UNII: 506T60A25R) 8.3 mg in 1 mL WATER (UNII: 059QF0KO0R) Other Ingredients Ingredient Kind Ingredient Name Quantity May contain HYDROCHLORIC ACID (UNII: QTT17582CB) May contain SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:52533-198-76 300 mL in 1 BAG Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 10/22/2013 Labeler - Cantrell Drug Company (035545763)
