nateglinide

Generic: nateglinide

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

Drug Facts

Product Profile

Brand Name nateglinide
Generic Name nateglinide
Labeler modavar pharmaceuticals llc
Dosage Form TABLET, COATED
Routes
ORAL
Active Ingredients

nateglinide 120 mg/1

Manufacturer
Modavar Pharmaceuticals LLC

Identifiers & Regulatory

Product NDC 72241-003
Product ID 72241-003_af81465b-5f49-4eeb-8122-ef7fe5d90ddc
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA206432
Listing Expiration 2026-12-31
Marketing Start 2021-08-19

Pharmacologic Class

Established (EPC)
glinide [epc]
Mechanism of Action
potassium channel antagonists [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72241003
Hyphenated Format 72241-003

Supplemental Identifiers

RxCUI
311919 314142
UNII
41X3PWK4O2
NUI
N0000175428 N0000175448

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 nateglinide (source: ndc)
Generic Name nateglinide (source: ndc)
Application Number ANDA206432 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 120 mg/1
source: ndc
Packaging
  • 90 TABLET, COATED in 1 BOTTLE (72241-003-04)
  • 100 TABLET, COATED in 1 BOTTLE (72241-003-05)
source: ndc

Packages (2)

Ingredients (1)

nateglinide (120 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "af81465b-5f49-4eeb-8122-ef7fe5d90ddc", "openfda": {"nui": ["N0000175428", "N0000175448"], "unii": ["41X3PWK4O2"], "rxcui": ["311919", "314142"], "spl_set_id": ["af81465b-5f49-4eeb-8122-ef7fe5d90ddc"], "pharm_class_epc": ["Glinide [EPC]"], "pharm_class_moa": ["Potassium Channel Antagonists [MoA]"], "manufacturer_name": ["Modavar Pharmaceuticals LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, COATED in 1 BOTTLE (72241-003-04)", "package_ndc": "72241-003-04", "marketing_start_date": "20210819"}, {"sample": false, "description": "100 TABLET, COATED in 1 BOTTLE (72241-003-05)", "package_ndc": "72241-003-05", "marketing_start_date": "20210819"}], "brand_name": "Nateglinide", "product_id": "72241-003_af81465b-5f49-4eeb-8122-ef7fe5d90ddc", "dosage_form": "TABLET, COATED", "pharm_class": ["Glinide [EPC]", "Potassium Channel Antagonists [MoA]"], "product_ndc": "72241-003", "generic_name": "Nateglinide", "labeler_name": "Modavar Pharmaceuticals LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Nateglinide", "active_ingredients": [{"name": "NATEGLINIDE", "strength": "120 mg/1"}], "application_number": "ANDA206432", "marketing_category": "ANDA", "marketing_start_date": "20210819", "listing_expiration_date": "20261231"}