NDC codes

FDA NDC Directory
Product NDC (as listed)73141-024Labeler and product segments. Claims need a package NDC.
Product NDC at billing width73141-0024Add 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 NDC11-digit (billing)PackageCopy
73141-024-02731410024027314100240260 TABLET, FILM COATED in 1 BOTTLE (73141-024-02)Marketed from May 16, 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)
Maraviroc
Generic name (nonproprietary)
maraviroc
Active ingredients
Maraviroc — 150 mg/1
Dosage form
Tablet, Film coated
Route
Oral
Labeler
A2A Integrated PharmaceuticalsNDC labeler code 73141
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 217114
Marketing start
Listing expires
Other FDA classes
Chemokine Co-receptor 5 Antagonists (Mechanism)
Identifiers
Product ID 73141-024_33a02559-b292-1860-e063-6394a90a8868SPL ID 33a02559-b292-1860-e063-6394a90a8868SPL set ID 2a16417d-a3b8-483b-9dfe-d5263cc16538RxCUI 728223, 728225UNII MD6P741W8AUPC 0373141024021, 0373141025028
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

N473141002402 followed by a unit qualifier and the quantity

Package 73141-0024-02. 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 . This label includes a boxed warning.

Indications (excerpt from the label)

Maraviroc is indicated in combination with other antiretroviral agents for the treatment of only CCR5‑tropic human immunodeficiency virus type 1 (HIV‑1) infection in adult and pediatric patients 2 years of age and older weighing at least 10 kg. Limitations of Use Maraviroc is not recommended in patients with dual/mixed- or CXCR4-tropic HIV- 1 [see Microbiology (12.4) ] . Maraviroc is a CCR5 co-receptor antagonist indicated in combination with other antiretroviral agents for the treatment of only CCR5-tropic HIV-1 infection in adults and pediatric patients 2 years of age and older weighing at least 10 kg. ( 1 ) Limitations of Use: Not recommended in patients with dual/mixed- or CXCR4-tropic H…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 73141-024

What is NDC 73141-024?
73141-024 is the product NDC for Maraviroc, Maraviroc 150 mg/1 tablet, film coated, listed with the FDA by A2A Integrated Pharmaceuticals. 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?
A2A Integrated Pharmaceuticals, NDC labeler code 73141. 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
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
MaravirocMaraviroc 150 mg/1Tablet, Film coatedOralRhodes Pharmaceuticals LLC42858-24642858-0246-06
MaravirocMaraviroc 300 mg/1Tablet, Film coatedOralRhodes Pharmaceuticals LLC42858-24742858-0247-06
MaravirocMaraviroc 300 mg/1Tablet, Film coatedOralNavinta LLC68475-00768475-0007-01
MaravirocMaraviroc 150 mg/1Tablet, Film coatedOralNavinta LLC68475-00868475-0008-01
MaravirocMaraviroc 150 mg/1Tablet, Film coatedOralZydus Pharmaceuticals USA Inc.70710-193070710-1930-06
MaravirocMaraviroc 300 mg/1Tablet, Film coatedOralZydus Pharmaceuticals USA Inc.70710-193170710-1931-06
MaravirocMaraviroc 300 mg/1Tablet, Film coatedOralA2A Integrated Pharmaceuticals73141-02573141-0025-02
MaravirocMaraviroc 150 mg/1Tablet, Film coatedOralA-S Medication Solutions50090-801050090-8010-00
MaravirocMaraviroc 150 mg/1Tablet, Film coatedOrali3 Pharmaceuticals, LLC72319-02472319-0024-02
MaravirocMaraviroc 300 mg/1Tablet, Film coatedOrali3 Pharmaceuticals, LLC72319-02572319-0025-02

All 16 Maraviroc NDCs

Other NDCs under ANDA 217114

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

FDA NDC Directory listings under ANDA 217114
ProductStrengthForm · routeLabelerProduct NDC
MaravirocMaraviroc 150 mg/1Tablet, Film coatedOralA-S Medication Solutions50090-8010
MaravirocMaraviroc 150 mg/1Tablet, Film coatedOrali3 Pharmaceuticals, LLC72319-024
MaravirocMaraviroc 300 mg/1Tablet, Film coatedOrali3 Pharmaceuticals, LLC72319-025
MaravirocMaraviroc 300 mg/1Tablet, Film coatedOralA2A Integrated Pharmaceuticals73141-025

Free account

Log in to keep searching

You’ve used your 3 free searches. Med-Code is free: log in or create a free profile to keep looking up NDCs, J-codes and drugs.

Create a free profileLog in