Physostigma Venenosum NDC 37662-2381

NDC codes

FDA NDC Directory

Product NDC (as listed)37662-2381Labeler and product segments. Claims need a package NDC.

Product NDC at billing width37662-2381Add 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
37662-2381-1	37662238101	200 PELLET in 1 VIAL, GLASS (37662-2381-1)Marketed from Jan 17, 2023
37662-2381-2	37662238102	1200 PELLET in 1 BOTTLE, GLASS (37662-2381-2)Marketed from Jan 17, 2023
37662-2381-3	37662238103	4000 PELLET in 1 BOTTLE, GLASS (37662-2381-3)Marketed from Jan 17, 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): Physostigma Venenosum
Generic name (nonproprietary): physostigma venenosum
Active ingredients: Physostigma venenosum seed — 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: Jan 17, 2023
Listing expires: Dec 31, 2026
Identifiers: Product ID 37662-2381_f27fbace-3f51-d282-e053-2995a90a9649SPL ID f27fbace-3f51-d282-e053-2995a90a9649SPL set ID f27fbace-3f50-d282-e053-2995a90a9649UNII CJV9E9IIOA

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

N437662238101 followed by a unit qualifier and the quantity

Package 37662-2381-01. 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 Jan 17, 2023.

Full label on DailyMed (opens in a new tab)