Lithium (lithium bromatum) NDC 60986-1019

NDC codes

FDA NDC Directory

Product NDC (as listed)60986-1019Labeler and product segments. Claims need a package NDC.

Product NDC at billing width60986-1019Add the package segment from the table below.

Package NDCs as listed with the FDA, and the 11-digit 5-4-2 form used on claims. The highlighted digit is the added leading zero.
Package NDC	11-digit (billing)	Package	Copy
60986-1019-3	60986101903	50 mL in 1 BOTTLE, GLASS (60986-1019-3)Marketed from Feb 28, 2018
60986-1019-4	60986101904	100 mL in 1 BOTTLE, GLASS (60986-1019-4)Marketed from Feb 28, 2018

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules

Product information

Brand name (proprietary): Lithium
Generic name (nonproprietary): lithium bromatum
Active ingredients: Lithium bromide — 3 [hp_X]/mL
Dosage form: Liquid
Route: Oral
Labeler: Marco Pharma International LLC.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Mar 1, 1992
Listing expires: Dec 31, 2027
Identifiers: Product ID 60986-1019_483c1e49-a5da-749f-e063-6394a90a226eSPL ID 483c1e49-a5da-749f-e063-6394a90a226eSPL set ID f4a1d451-33ad-4df3-ae68-58cfbfccfa89UNII 864G646I84
Pharmacologic class: Mood Stabilizer

Billing references

What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.

HCPCS codeNo match

No HCPCS code in Med-Code's directory. Oral products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N460986101903 followed by a unit qualifier and the quantity

Package 60986-1019-03. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier

Product label

Current FDA label (SPL), effective Jan 12, 2026.

Indications (excerpt from the label)

Dosage Adults: Take 20 drops on the toungue or in water two to three times daily. Children receive 1/2 of the adult amount.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)