Home NDC 73442-0001 FUCIDIN
Product NDC 73442-0001
11-digit product format 734420001
Labeler code 73442
Product ID 73442-0001_96b7b864-2571-8570-e053-2995a90a176b
Type HUMAN OTC DRUG
Nonproprietary name Sodium Fusidate
Dosage form OINTMENT
Route TOPICAL
Labeler I World Pharmaceutical Co., Ltd.
Marketing category UNAPPROVED DRUG OTHER
Marketing start 2019-10-08
Marketing end 0000-00-00
Substance FUSIDATE SODIUM
Active strength 20 mg/g
NDC exclude flag No
Listing certified through 2020-12-31
Current FDA listing Historical FDA.report record Observed NDC auxiliary status history# This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
Historic NDC status page 1 of 1 · 10 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Package NDC Code Status Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 excluded product product D Discontinued by firm d630ba8d3edf…732f749b63fb…2025-12-14 17:58 UTC · source 2025-12-05 excluded package package 73442-0001-1 D Discontinued by firm d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 excluded product product D Discontinued by firm f5e01cc5f278…a2eaf40c39c3…2025-08-27 00:01 UTC · source 2025-08-26 excluded package package 73442-0001-1 D Discontinued by firm f5e01cc5f278…a2eaf40c39c3…2025-02-02 03:52 UTC · source 2025-01-31 excluded product product U Excluded because listing certification expired 302b2466d912…e7b80fea0513…2025-02-02 03:52 UTC · source 2025-01-31 excluded package package 73442-0001-1 U Excluded because listing certification expired 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 excluded product product U Excluded because listing certification expired ed331223b511…672a5bd82f5f…2025-01-20 13:05 UTC · source 2025-01-20 excluded package package 73442-0001-1 U Excluded because listing certification expired ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 excluded product product U Excluded because listing certification expired 0efc9e666f02…f202fb6c5f17…2025-01-11 03:41 UTC · source 2025-01-10 excluded package package 73442-0001-1 U Excluded because listing certification expired 0efc9e666f02…f202fb6c5f17…
FDA-Initiated Inactive NDC Indexing# DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 73442-0001 FUCIDIN (SODIUM FUSIDATE) OINTMENT [I WORLD PHARMACEUTICAL CO., LTD.] 2 Legacy NDC 20250215_96b7b841-0954-85a2-e053-2995a90aafdf.zip
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 73442-0001-1 73442000101 10 g in 1 TUBE (73442-0001-1) 10 g 2019-10-08 0000-00-00 No No Current