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 NDC11-digit (billing)PackageCopy
60986-1019-3609861019036098610190350 mL in 1 BOTTLE, GLASS (60986-1019-3)Marketed from Feb 28, 2018
60986-1019-46098610190460986101904100 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.NDC labeler code 60986
Product type
Over-the-counter drug
Marketing category
Unapproved homeopathic
Marketing start
Listing expires
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 .

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)

About NDC 60986-1019

What is NDC 60986-1019?
60986-1019 is the product NDC for Lithium (lithium bromatum), Lithium bromide 3 [hp_X]/mL liquid, listed with the FDA by Marco Pharma International LLC.. It has 2 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Lithium (Lithium Bromatum).
What is the active ingredient?
Lithium bromide.
Who is the labeler?
Marco Pharma International LLC., NDC labeler code 60986. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Lithium?
7 other product NDCs are listed under this name. See all Lithium NDCs.
Is there a related HCPCS / J-code?
Not in Med-Code's curated HCPCS directory. See Billing references above.

Other finished products listed under the same name: strengths, forms and labelers.

Other Lithium NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
LithiumLithium citrate 8 meq/5mLSolutionOralPAI Holdings, LLC dba PAI Pharma0121-102700121-1027-16
LithiumLithium citrate 8 meq/5mLSolutionOralPAI Holdings, LLC dba PAI Pharma0121-402700121-4027-94
Lithiumlithium citrateLithium citrate 8 meq/5mLSolutionOralPrecision Dose, Inc.68094-07768094-0077-62
LithiumLithium citrate 8 meq/5mLSolutionOralREMEDYREPACK INC.70518-422770518-4227-0070518-4227-02
LithiumLithium citrate 8 meq/5mLSolutionOralSaptalis Pharmaceuticals, LLC71656-07271656-0072-1671656-0072-50
LithiumLithium citrate 8 meq/5mLSolutionOralAdvagen Pharma Ltd72888-17272888-0172-46
LithiumLithium citrate 8 meq/5mLSolutionOralAtlantic Biologicals Corp.17856-117217856-1172-01

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