Label: AX PHARMACEUTICAL CORP- tolazoline hydrochloride powder
- NDC Code(s): 62157-473-01
- Packager: AX Pharmaceutical Corp
- Category: BULK INGREDIENT
- DEA Schedule: None
- Marketing Status: Bulk Ingredient For Animal Drug Compounding
Drug Label Information
Updated August 23, 2017
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INGREDIENTS AND APPEARANCE
AX PHARMACEUTICAL CORP
tolazoline hydrochloride powderProduct Information Product Type BULK INGREDIENT Item Code (Source) NDC:62157-473 Route of Administration NOT APPLICABLE Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength TOLAZOLINE HYDROCHLORIDE (UNII: E669Z6S1JG) (TOLAZOLINE - UNII:CHH9H12AQ3) TOLAZOLINE 495 g in 500 g Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) Product Characteristics Color white Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:62157-473-01 500 g in 1 JAR 08/22/2017 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date bulk ingredient for animal drug compounding 08/22/2017 Labeler - AX Pharmaceutical Corp (202924858) Establishment Name Address ID/FEI Business Operations AX Pharmaceutical Corp 202924858 repack(62157-473) , relabel(62157-473)