Xylazine Hydrochloride

Manufacturer: Medisca Inc.
Effective date: 2013-01-11
Label type: BULK INGREDIENT
Version: 1
Source: legacy-cache
Hydrated at: 2026-08-02 01:42:18

Label at a glance#

ProductXylazine Hydrochloride

Active ingredientXYLAZINE HYDROCHLORIDE

Label structure1 sections

Contacts and useful links#

PhoneLabel contact1 (800) 932-1039

Label contents#

Full prescribing information#

Xylazine Hydrochloride, USP

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

DESCRIPTION: Colorless to white crystals

NDC 38779-2419-5

Packed by Medisca Inc.

Plattsburgh, NY, 12901, USA

MEDISCA

TO ORDER CALL 1 (800) 932-1039

XYLAZINE HYDROCHLORIDE, USP

Caution: Not For Human Use

100 g

For use and distribution in prescription compounding, manufacturing, processing or repacking only in accordance with FDA regulations and applicable law.

STORAGE: Preserve in tight containers. Store at 25°C, excursions permitted between 15°-30°C.

Lot:

Exp:

Cas: 23076-35-9

See Material Safety Data Sheet

image description

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
38779-2419-5	GM - Gram	38779-2419	68de19b7-17f1-4670-a067-5629fea30ec2	1	2015-10-02
38779-2419-9	GM - Gram	38779-2419	14243d6f-9f22-49b3-983c-89a48e523907	1	2015-10-02

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	SPL version	Uploaded
XYLAZINE HYDROCHLORIDE	ACTIVE INGREDIENT	NGC3S0882S	1
XYLAZINE	ACTIVE MOIETY	2KFG9TP5V8	1

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 2 matching rows.

Xylazine Hydrochloride
XYLAZINE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
38779-2419	38779-2419-5, 38779-2419-9

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 1 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
XYLAZINE HYDROCHLORIDE	NGC3S0882S	ACTIB

Source Document#

Source XML

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.