Tacrolimus (Page 12 of 12)

TACROLIMUS

Label ImageLabel Image
TACROLIMUS
tacrolimus capsule
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:50090-5596(NDC:0781-2103)
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
TACROLIMUS (TACROLIMUS ANHYDROUS) TACROLIMUS ANHYDROUS 1 mg
Inactive Ingredients
Ingredient Name Strength
CROSCARMELLOSE SODIUM
HYPROMELLOSE 2208 (100 MPA.S)
LACTOSE MONOHYDRATE
MAGNESIUM STEARATE
FERROSOFERRIC OXIDE
GELATIN, UNSPECIFIED
FERRIC OXIDE RED
TITANIUM DIOXIDE
FERRIC OXIDE YELLOW
AMMONIA
POTASSIUM HYDROXIDE
PROPYLENE GLYCOL
SHELLAC
BUTYL ALCOHOL
Product Characteristics
Color WHITE (white opaque body and brown cap) Score no score
Shape CAPSULE Size 14mm
Flavor Imprint Code 644;S
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:50090-5596-0 90 CAPSULE in 1 BOTTLE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA065461 08/10/2009
Labeler — A-S Medication Solutions (830016429)
Establishment
Name Address ID/FEI Operations
A-S Medication Solutions 830016429 RELABEL (50090-5596), REPACK (50090-5596)

Revised: 09/2021 A-S Medication Solutions

All MedLibrary.org resources are included in as near-original form as possible, meaning that the information from the original provider has been rendered here with only typographical or stylistic modifications and not with any substantive alterations of content, meaning or intent.

This site is provided for educational and informational purposes only, in accordance with our Terms of Use, and is not intended as a substitute for the advice of a medical doctor, nurse, nurse practitioner or other qualified health professional.

Privacy Policy | Copyright © 2022. All Rights Reserved.