Home NDC 43742-1642 Brucella Homochord
Product NDC 43742-1642
11-digit product format 437421642
Labeler code 43742
Product ID 43742-1642_c68ed65b-6733-455f-b17e-4a205525ae82
Type HUMAN OTC DRUG
Nonproprietary name Brucella Melitensis
Dosage form LIQUID
Route ORAL
Labeler Deseret Biologicals, Inc.
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2020-03-31
Marketing end 2025-03-31
Substance BRUCELLA MELITENSIS
Active strength 18 [hp_C]/mL
NDC exclude flag No
Listing certified through 0000-00-00
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 · 4 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Package NDC Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 excluded product product d630ba8d3edf…732f749b63fb…2025-12-14 17:58 UTC · source 2025-12-05 excluded package package 43742-1642-1 d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 excluded product product f5e01cc5f278…a2eaf40c39c3…2025-08-27 00:01 UTC · source 2025-08-26 excluded package package 43742-1642-1 f5e01cc5f278…a2eaf40c39c3…
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 43742-1642-1 43742164201 30 mL in 1 BOTTLE, DROPPER (43742-1642-1) 30 ml 2020-03-31 2025-03-31 No No Current