Manganum Oxydatum Nigrum NDC 37662-2855

NDC codes

FDA NDC Directory

Product NDC (as listed)37662-2855Labeler and product segments. Claims need a package NDC.

Product NDC at billing width37662-2855Add 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
37662-2855-1	37662285501	200 PELLET in 1 VIAL, GLASS (37662-2855-1)Marketed from Mar 28, 2023
37662-2855-2	37662285502	1200 PELLET in 1 BOTTLE, GLASS (37662-2855-2)Marketed from Mar 28, 2023
37662-2855-3	37662285503	4000 PELLET in 1 BOTTLE, GLASS (37662-2855-3)Marketed from Mar 28, 2023

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): Manganum Oxydatum Nigrum
Generic name (nonproprietary): manganum oxydatum nigrum
Active ingredients: Manganese dioxide — 12 [hp_C]/1
Dosage form: Pellet
Route: Oral
Labeler: Hahnemann Laboratories, INC.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Mar 28, 2023
Listing expires: Dec 31, 2026
Identifiers: Product ID 37662-2855_f7f1948a-6d76-368b-e053-6294a90a39c6SPL ID f7f1948a-6d76-368b-e053-6294a90a39c6SPL set ID f7f1948a-6d75-368b-e053-6294a90a39c6UNII TF219GU161

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

N437662285501 followed by a unit qualifier and the quantity

Package 37662-2855-01. 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 Mar 28, 2023.

Full label on DailyMed (opens in a new tab)