Home NDC 60986-1019-3 Lithium
Product NDC 60986-1019
Requested package NDC 60986-1019-3
11-digit product format 609861019
Labeler code 60986
Product ID 60986-1019_483c1e49-a5da-749f-e063-6394a90a226e
Type HUMAN OTC DRUG
Nonproprietary name Lithium Bromatum
Dosage form LIQUID
Route ORAL
Labeler Marco Pharma International LLC.
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 1992-03-01
Substance LITHIUM BROMIDE
Active strength 3 [hp_X]/mL
Pharmacologic classes Mood Stabilizer [EPC]
NDC exclude flag No
Listing certified through 2027-12-31
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 2020-06-10 20:45 UTC · source 2020-06-10 excluded package package 60986-1019 60986-1019-3 I Inactivated by FDA excluded / ndc_excluded.zip 9bebd1f3094a…5416666fcb17…
Additional Listing Data#
Finished product Yes
Brand name base Lithium
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength LITHIUM BROMIDE 3 [hp_X]/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 864G646I84 Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 60986-1019-3 Lithium 50 mL in 1 BOTTLE, GLASS LIQUID 50 6 60986-1019-4 Lithium 100 mL in 1 BOTTLE, GLASS LIQUID 100 6
DailyMed Socrata Ingredients# DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 60986-1019 LITHIUM (LITHIUM BROMATUM) LIQUID [MARCO PHARMA INTERNATIONAL LLC.] 5 Current NDC, Legacy NDC, 2 package rows 20241206_f4a1d451-33ad-4df3-ae68-58cfbfccfa89.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 60986-1019-3 60986101903 50 mL in 1 BOTTLE, GLASS (60986-1019-3) 50 ml 2018-02-28 0000-00-00 No No Current