Label: SELEGILINE HYDROCHLORIDE powder
- NDC Code(s): 73377-012-01, 73377-012-02
- Packager: AX Pharmaceutical Corp
- Category: BULK INGREDIENT
- DEA Schedule: None
- Marketing Status: Bulk Ingredient For Animal Drug Compounding
Drug Label Information
Updated February 4, 2020
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Selegiline Hydrochloride
-
INGREDIENTS AND APPEARANCE
SELEGILINE HYDROCHLORIDE
selegiline hydrochloride powderProduct Information Product Type BULK INGREDIENT Item Code (Source) NDC:73377-012 Route of Administration NOT APPLICABLE Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SELEGILINE HYDROCHLORIDE (UNII: 6W731X367Q) (SELEGILINE HYDROCHLORIDE - UNII:6W731X367Q) SELEGILINE HYDROCHLORIDE 1 g in 1 g Product Characteristics Color white Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:73377-012-01 500 g in 1 JAR 02/04/2020 2 NDC:73377-012-02 100 g in 1 JAR 03/06/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date bulk ingredient for animal drug compounding 02/04/2020 Labeler - AX Pharmaceutical Corp (204011316) Establishment Name Address ID/FEI Business Operations AX Pharmaceutical Corp 204011316 repack(73377-012) , relabel(73377-012)
