Coffea Cruda 200ck (arabica coffee bean) NDC 76472-3013

NDC codes

FDA NDC Directory

Product NDC (as listed)76472-3013Labeler and product segments. Claims need a package NDC.

Product NDC at billing width76472-3013Add 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
76472-3013-1	76472301301	80 PELLET in 1 CYLINDER (76472-3013-1)Marketed from Nov 24, 2011

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): Coffea Cruda 200ckSuffix: 200ck
Generic name (nonproprietary): arabica coffee bean
Active ingredients: Arabica coffee bean — 200 [kp_C]/1
Dosage form: Pellet
Route: Sublingual
Labeler: SEVENE USA
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Nov 24, 2011
Listing expires: Dec 31, 2026
Other FDA classes: Allergens (Chemical structure)Cell-mediated Immunity (Physiologic effect)Dietary Proteins (Chemical structure)Increased Histamine Release (Physiologic effect)Plant Proteins (Chemical structure)Seed Storage Proteins (Chemical structure)
Identifiers: Product ID 76472-3013_2ddc3aac-ab42-ef41-e063-6394a90a04d6SPL ID 2ddc3aac-ab42-ef41-e063-6394a90a04d6SPL set ID c8d62cad-5580-86ae-e053-2995a90a8987UNII 3SW678MX72UPC 0850022941320
Pharmacologic class: Non-Standardized Food Allergenic Extract; Non-Standardized Plant Allergenic Extract

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. Sublingual products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N476472301301 followed by a unit qualifier and the quantity

Package 76472-3013-01. 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 Feb 11, 2025.

Indications (excerpt from the label)

USE: Condition listed above or as directed by a physician.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)