What is NDC 59651-646?

59651-646 is the product NDC for Mycophenolate Mofetil, Mycophenolate mofetil 200 mg/mL powder, for suspension, listed with the FDA by Aurobindo Pharma Limited. It has 1 package NDC, shown above in 10- and 11-digit form.

Aurobindo Pharma Limited, NDC labeler code 59651. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Mycophenolate Mofetil?

57 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

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	5965106462659651064626	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 LimitedNDC labeler code 59651
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.

About NDC 59651-646

What is NDC 59651-646?: 59651-646 is the product NDC for Mycophenolate Mofetil, Mycophenolate mofetil 200 mg/mL powder, for suspension, listed with the FDA by Aurobindo Pharma Limited. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Mycophenolate Mofetil.
What is the active ingredient?: Mycophenolate mofetil.
Who is the labeler?: Aurobindo Pharma Limited, NDC labeler code 59651. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Mycophenolate Mofetil?: 57 other product NDCs are listed under this name. See all Mycophenolate Mofetil 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 Mycophenolate Mofetil NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
mycophenolate mofetil	Mycophenolate mofetil 250 mg/1	CapsuleOral	Cardinal Health 107, LLC	55154-0161	55154-0161-00
Mycophenolate Mofetil	Mycophenolate mofetil 200 mg/mL	Powder, For suspensionOral	Strides Pharma Science Limited	64380-899	64380-0899-00
Mycophenolate Mofetil	Mycophenolate mofetil 200 mg/mL	Powder, For suspensionOral	QUAGEN PHARMACEUTICALS LLC	70752-294	70752-0294-60
Mycophenolate Mofetil	Mycophenolate mofetil 200 mg/mL	Powder, For suspensionOral	NorthStar Rx LLC	72603-751	72603-0751-01
mycophenolate mofetil	Mycophenolate mofetil 250 mg/1	CapsuleOral	Major Pharmaceuticals	0904-7466	00904-7466-61
Mycophenolate Mofetil	Mycophenolate mofetil 250 mg/1	CapsuleOral	Wuxi Fortune Pharmaceutical Co.,Ltd.	65050-2073	65050-2073-00
Mycophenolate mofetil	Mycophenolate mofetil 500 mg/1	Tablet, Film coatedOral	REMEDYREPACK INC.	70518-4377	70518-4377-00
Mycophenolate mofetil	Mycophenolate mofetil 250 mg/1	CapsuleOral	AvKARE	73190-009	73190-0009-0173190-0009-50
Mycophenolate mofetil	Mycophenolate mofetil 500 mg/1	Tablet, Film coatedOral	AvKARE	73190-010	73190-0010-0173190-0010-50
mycophenolate mofetil	Mycophenolate mofetil 250 mg/1	CapsuleOral	American Health Packaging	60687-885	60687-0885-01

All 58 Mycophenolate Mofetil NDCs

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