maraviroc

Generic: maraviroc

Labeler: i3 pharmaceuticals, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name maraviroc
Generic Name maraviroc
Labeler i3 pharmaceuticals, llc
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

maraviroc 150 mg/1

Manufacturer
i3 Pharmaceuticals, LLC

Identifiers & Regulatory

Product NDC 72319-024
Product ID 72319-024_0416607a-fd74-87e3-e063-6294a90ae6b5
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA217114
Listing Expiration 2026-12-31
Marketing Start 2023-09-15

Pharmacologic Class

Established (EPC)
ccr5 co-receptor antagonist [epc]
Mechanism of Action
chemokine co-receptor 5 antagonists [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72319024
Hyphenated Format 72319-024

Supplemental Identifiers

RxCUI
728223 728225
UPC
0372319024023 0372319025020
UNII
MD6P741W8A
NUI
N0000175572 N0000175445

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name maraviroc (source: ndc)
Generic Name maraviroc (source: ndc)
Application Number ANDA217114 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 150 mg/1
source: ndc
Packaging
  • 60 TABLET, FILM COATED in 1 BOTTLE (72319-024-02)
source: ndc

Packages (1)

72319-024-02 60 TABLET, FILM COATED in 1 BOTTLE (72319-024-02)

Ingredients (1)

maraviroc (150 mg/1)

Linked Drug Pages (1)

Maraviroc ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "0416607a-fd74-87e3-e063-6294a90ae6b5", "openfda": {"nui": ["N0000175572", "N0000175445"], "upc": ["0372319024023", "0372319025020"], "unii": ["MD6P741W8A"], "rxcui": ["728223", "728225"], "spl_set_id": ["f7b9c67b-10c6-45b5-b2a8-952cd350b0b1"], "pharm_class_epc": ["CCR5 Co-receptor Antagonist [EPC]"], "pharm_class_moa": ["Chemokine Co-receptor 5 Antagonists [MoA]"], "manufacturer_name": ["i3 Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (72319-024-02)", "package_ndc": "72319-024-02", "marketing_start_date": "20230915"}], "brand_name": "Maraviroc", "product_id": "72319-024_0416607a-fd74-87e3-e063-6294a90ae6b5", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["CCR5 Co-receptor Antagonist [EPC]", "Chemokine Co-receptor 5 Antagonists [MoA]"], "product_ndc": "72319-024", "generic_name": "Maraviroc", "labeler_name": "i3 Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Maraviroc", "active_ingredients": [{"name": "MARAVIROC", "strength": "150 mg/1"}], "application_number": "ANDA217114", "marketing_category": "ANDA", "marketing_start_date": "20230915", "listing_expiration_date": "20261231"}