What is NDC 70518-4036?

70518-4036 is the product NDC for Mycophenolate Mofetil, Mycophenolate mofetil 250 mg/1 capsule, listed with the FDA by REMEDYREPACK INC.. It has 1 package NDC, shown above in 10- and 11-digit form.

REMEDYREPACK INC., NDC labeler code 70518. 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 70518-4036

NDC codes

FDA NDC Directory

Product NDC (as listed)70518-4036Labeler and product segments. Claims need a package NDC.

Product NDC at billing width70518-4036Add 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
70518-4036-0	7051840360070518403600	100 POUCH in 1 BOX (70518-4036-0) / 1 CAPSULE in 1 POUCH (70518-4036-1)Marketed from Mar 11, 2024

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): Mycophenolate Mofetil
Generic name (nonproprietary): mycophenolate mofetil
Active ingredients: Mycophenolate mofetil — 250 mg/1
Dosage form: Capsule
Route: Oral
Labeler: REMEDYREPACK INC.NDC labeler code 70518
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 210181
Marketing start: Mar 11, 2024
Listing expires: Dec 31, 2027
Identifiers: Product ID 70518-4036_54115d78-da38-7539-e063-6294a90ab0dcSPL ID 54115d78-da38-7539-e063-6294a90ab0dcSPL set ID d203775c-bf36-460c-bacf-3ab2348a514fRxCUI 199058UNII 9242ECW6R0
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

N470518403600 followed by a unit qualifier and the quantity

Package 70518-4036-00. 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 Jun 12, 2026. This label includes a boxed warning.

Indications (excerpt from the label)

Mycophenolate mofetil is an antimetabolite immunosuppressant indicated for the prophylaxis of organ rejection in adult and pediatric recipients 3 months of age and older of allogeneic kidney, heart or liver transplants, in combination with other immunosuppressants. ( 1 ) Mycophenolate mofetil (MMF) is indicated for the prophylaxis of organ rejection, in adult and pediatric recipients 3 months of age and older of allogeneic kidney [see Clinical Studies (14.1) ] , heart [see Clinical Studies (14.2) ] or liver transplants [see Clinical Studies (14.3) ], in combination with other immunosuppressants.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 70518-4036

What is NDC 70518-4036?: 70518-4036 is the product NDC for Mycophenolate Mofetil, Mycophenolate mofetil 250 mg/1 capsule, listed with the FDA by REMEDYREPACK INC.. 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?: REMEDYREPACK INC., NDC labeler code 70518. 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 210181

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

FDA NDC Directory listings under ANDA 210181
Product	Strength	Form · route	Labeler	Product NDC
Mycophenolate Mofetil	Mycophenolate mofetil 250 mg/1	CapsuleOral	CONCORD BIOTECH LIMITED	68254-5000
Mycophenolate Mofetil	Mycophenolate mofetil 250 mg/1	CapsuleOral	Advagen Pharma Limited	72888-192