What is NDC 42858-247?

42858-247 is the product NDC for Maraviroc, Maraviroc 300 mg/1 tablet, film coated, listed with the FDA by Rhodes Pharmaceuticals LLC. It has 1 package NDC, shown above in 10- and 11-digit form.

Rhodes Pharmaceuticals LLC, NDC labeler code 42858. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Maraviroc?

15 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Maraviroc NDC 42858-247 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)42858-247Labeler and product segments. Claims need a package NDC.

Product NDC at billing width42858-0247Add 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
42858-247-06	42858024706	60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (42858-247-06)Marketed from Sep 30, 2026

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): Maraviroc
Generic name (nonproprietary): maraviroc
Active ingredients: Maraviroc — 300 mg/1
Dosage form: Tablet, Film coated
Route: Oral
Labeler: Rhodes Pharmaceuticals LLCNDC labeler code 42858
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 216143
Marketing start: Sep 30, 2026
Listing expires: Dec 31, 2027
Other FDA classes: Chemokine Co-receptor 5 Antagonists (Mechanism)
Identifiers: Product ID 42858-247_7f97db4c-6c65-4056-b301-53feac86d8f4SPL ID 7f97db4c-6c65-4056-b301-53feac86d8f4
Pharmacologic class: CCR5 Co-receptor Antagonist

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

N442858024706 followed by a unit qualifier and the quantity

Package 42858-0247-06. 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 42858-247

What is NDC 42858-247?: 42858-247 is the product NDC for Maraviroc, Maraviroc 300 mg/1 tablet, film coated, listed with the FDA by Rhodes Pharmaceuticals LLC. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Maraviroc.
What is the active ingredient?: Maraviroc.
Who is the labeler?: Rhodes Pharmaceuticals LLC, NDC labeler code 42858. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Maraviroc?: 15 other product NDCs are listed under this name. See all Maraviroc 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 Maraviroc NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Maraviroc	Maraviroc 150 mg/1	Tablet, Film coatedOral	Rhodes Pharmaceuticals LLC	42858-246	42858-0246-06
Maraviroc	Maraviroc 300 mg/1	Tablet, Film coatedOral	Navinta LLC	68475-007	68475-0007-01
Maraviroc	Maraviroc 150 mg/1	Tablet, Film coatedOral	Navinta LLC	68475-008	68475-0008-01
Maraviroc	Maraviroc 150 mg/1	Tablet, Film coatedOral	Zydus Pharmaceuticals USA Inc.	70710-1930	70710-1930-06
Maraviroc	Maraviroc 300 mg/1	Tablet, Film coatedOral	Zydus Pharmaceuticals USA Inc.	70710-1931	70710-1931-06
Maraviroc	Maraviroc 150 mg/1	Tablet, Film coatedOral	A2A Integrated Pharmaceuticals	73141-024	73141-0024-02
Maraviroc	Maraviroc 300 mg/1	Tablet, Film coatedOral	A2A Integrated Pharmaceuticals	73141-025	73141-0025-02
Maraviroc	Maraviroc 150 mg/1	Tablet, Film coatedOral	A-S Medication Solutions	50090-8010	50090-8010-00
Maraviroc	Maraviroc 150 mg/1	Tablet, Film coatedOral	i3 Pharmaceuticals, LLC	72319-024	72319-0024-02
Maraviroc	Maraviroc 300 mg/1	Tablet, Film coatedOral	i3 Pharmaceuticals, LLC	72319-025	72319-0025-02

All 16 Maraviroc NDCs

Other NDCs under ANDA 216143

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

FDA NDC Directory listings under ANDA 216143
Product	Strength	Form · route	Labeler	Product NDC
Maraviroc	Maraviroc 150 mg/1	Tablet, Film coatedOral	Rhodes Pharmaceuticals LLC	42858-246