Label: ISOTRETINOIN powder
- Label RSS
- Share
- NDC Code(s): 62157-877-01
- Packager: AX Pharmaceutical Corp
- Category: BULK INGREDIENT
- DEA Schedule: None
- Marketing Status: Bulk Ingredient For Animal Drug Compounding
Drug Label Information
Updated July 3, 2019
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Isotretinoin
-
INGREDIENTS AND APPEARANCE
ISOTRETINOIN
isotretinoin powderProduct Information Product Type BULK INGREDIENT Item Code (Source) NDC:62157-877 Route of Administration NOT APPLICABLE Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ISOTRETINOIN (UNII: EH28UP18IF) (ISOTRETINOIN - UNII:EH28UP18IF) ISOTRETINOIN 1 g in 1 g Product Characteristics Color yellow Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:62157-877-01 500 g in 1 JAR 07/03/2019 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date bulk ingredient for animal drug compounding 07/03/2019 Labeler - AX Pharmaceutical Corp (202924858) Establishment Name Address ID/FEI Business Operations AX Pharmaceutical Corp 202924858 relabel(62157-877) , repack(62157-877)
