Mycophenolate Mofetil NDC 59651-646

NDC codes

FDA NDC Directory

Product NDC (as listed)59651-646Labeler and product segments. Claims need a package NDC.

Product NDC at billing width59651-0646Add 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
59651-646-26	59651064626	1 BOTTLE in 1 CARTON (59651-646-26) / 225 mL in 1 BOTTLEMarketed from Sep 26, 2024

How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 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): Mycophenolate Mofetil
Generic name (nonproprietary): mycophenolate mofetil
Active ingredients: Mycophenolate mofetil — 200 mg/mL
Dosage form: Powder, For suspension
Route: Oral
Labeler: Aurobindo Pharma Limited
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 218227
Marketing start: Sep 26, 2024
Listing expires: Dec 31, 2027
Identifiers: Product ID 59651-646_8a61f3b8-01d2-4e75-b828-4fc3a8c495f2SPL ID 8a61f3b8-01d2-4e75-b828-4fc3a8c495f2
Pharmacologic class: Antimetabolite Immunosuppressant

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

N459651064626 followed by a unit qualifier and the quantity

Package 59651-0646-26. 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

The FDA listing for this product does not reference a label (SPL) set.

Other NDCs under ANDA 218227

Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.

FDA NDC Directory listings under ANDA 218227
Product	Strength	Form · route	Labeler	Product NDC
Mycophenolate Mofetil	Mycophenolate mofetil 200 mg/mL	Powder, For suspensionOral	NorthStar Rx LLC	72603-751