Protopic

Product NDC
50222-211
11-digit product format
502220211
Labeler code
50222
Product ID
50222-211_f859e9b6-d4c5-472e-b165-24a05897dd79
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Tacrolimus
Dosage form
OINTMENT
Route
TOPICAL
Labeler
LEO Pharma Inc
Application
NDA050777
Marketing category
NDA
Marketing start
2000-12-08
Marketing end
2024-12-31
Substance
TACROLIMUS
Active strength
1 mg/g
Pharmacologic classes
Calcineurin Inhibitor Immunosuppressant [EPC], Calcineurin Inhibitors [MoA]
NDC exclude flag
No
Listing certified through
0000-00-00
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
50222-211-10GM - Gram50222-21131391ed5-1dad-4e04-b7a8-825994bbdb0112017-03-06
50222-211-30GM - Gram50222-2110fa960e8-c56a-42e7-867b-21ebfb9e011512017-03-06
50222-211-60GM - Gram50222-211d9a95a94-c3db-4487-aaf8-f071899c678212017-03-06

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
50222-211-10502220211101 TUBE in 1 CARTON (50222-211-10) > 100 g in 1 TUBE1 tube2016-08-190000-00-00NoNoCurrent
50222-211-30502220211301 TUBE in 1 CARTON (50222-211-30) > 30 g in 1 TUBE1 tube2016-08-190000-00-00NoNoCurrent
50222-211-60502220211601 TUBE in 1 CARTON (50222-211-60) > 60 g in 1 TUBE1 tube2016-08-190000-00-00NoNoCurrent