Label: TYLOSIN PHOSPHATE powder
-
Contains inactivated NDC Code(s)
NDC Code(s): 11311-799-25 - Packager: Biovet Joint Stock Company
- Category: BULK INGREDIENT - ANIMAL DRUG
- DEA Schedule: None
- Marketing Status: bulk ingredient
Drug Label Information
Updated January 12, 2022
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
-
DRUM LABEL
TYLOSIN PHOSPHATE
ACTIVE PHARMACEUTICAL INGREDIENT
BATCH No:
NET WEIGHT:
GROSS WEIGHT:
MANUFACTURE DATE:
EXPIRATION DATE:STORE AT OR BELOW 25°C, EXCURSIONS PERMITTED BEWTWEEN 15°C and 30°C.
PRESERVE IN WELL-CLOSED CONTAINER, PROTECTED FROM LIGHT, MOISTURE,AND EXCESSIVE HEAT.
FOR MANUFACTURING, PROCESSING OR REPACKING.
FOR ANIMAL USE ONLY!
PRODUCT MANUFACTURED IN BULGARIA
MANUFACTURED BY:
BIOVET JSC., 39 Petar Rakov St.,Peshtera 4550, Bulgaria
- Drum Label Image
-
INGREDIENTS AND APPEARANCE
TYLOSIN PHOSPHATE
tylosin phosphate powderProduct Information Product Type Item Code (Source) NDC:11311-799 Route of Administration NOT APPLICABLE Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength TYLOSIN PHOSPHATE (UNII: NR75X12AFF) (TYLOSIN - UNII:YEF4JXN031) TYLOSIN 1 kg in 1 kg Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:11311-799-25 25 kg in 1 DRUM Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date bulk ingredient 05/29/2009 Labeler - Biovet Joint Stock Company (645015512) Registrant - Biovet Joint Stock Company (645015512) Establishment Name Address ID/FEI Business Operations Biovet Joint Stock Company 645015512 api manufacture, analysis
