Home NDC 15631-0248-4 KALI BROMATUM
Product NDC 15631-0248
Requested package NDC 15631-0248-4
11-digit product format 156310248
Labeler code 15631
Product ID 15631-0248_cd4f7ba3-554a-4e79-e053-2995a90adc42
Type HUMAN OTC DRUG
Nonproprietary name KALI BROMATUM
Dosage form PELLET
Route ORAL
Labeler Rxhomeo Private Limited d.b.a. Rxhomeo, Inc
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2015-09-03
Substance POTASSIUM BROMIDE
Active strength 1 [hp_X]/1
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes 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 · 1 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Product NDC Package NDC Code Status Reporting period Archive Snapshot Source SHA-256 2019-12-08 06:16 UTC · source 2019-12-05 excluded package package 15631-0248 15631-0248-4 E Excluded after deficient or non-compliant submission was not corrected excluded / ndc_excluded.zip 110d247fa046…a55b01930146…
Additional Listing Data#
Finished product Yes
Brand name base KALI BROMATUM
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength POTASSIUM BROMIDE 1 [hp_X]/1
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination OSD78555ZM Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# DailyMed Socrata Ingredients# DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 15631-0248 KALI BROMATUM PELLET [RXHOMEO PRIVATE LIMITED D.B.A. RXHOMEO, INC] 3 Current NDC, Legacy NDC, 8 package rows 20211003_04572087-c0c2-4ed9-8836-a159a62f1bf4.zip
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 1 of 1 · 1 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 15631-0248-4 15631024804 2500 PELLET in 1 PACKAGE (15631-0248-4) 2500 pellet 2018-01-01 0000-00-00 No No Current