nateglinide

Generic: nateglinide

Labeler: cadila pharmaceuticals limited
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name nateglinide
Generic Name nateglinide
Labeler cadila pharmaceuticals limited
Dosage Form TABLET, COATED
Routes
ORAL
Active Ingredients

nateglinide 60 mg/1

Manufacturer
Cadila Pharmaceuticals Limited

Identifiers & Regulatory

Product NDC 71209-030
Product ID 71209-030_efa28dcf-77d5-4fb2-b6c0-4939a9bf4766
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA206432
Listing Expiration 2026-12-31
Marketing Start 2014-02-10

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 71209030
Hyphenated Format 71209-030

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
  • 60 mg/1
source: ndc
Packaging
  • 90 TABLET, COATED in 1 BOTTLE (71209-030-04)
  • 100 TABLET, COATED in 1 BOTTLE (71209-030-05)
source: ndc

Packages (2)

71209-030-04 90 TABLET, COATED in 1 BOTTLE (71209-030-04) 71209-030-05 100 TABLET, COATED in 1 BOTTLE (71209-030-05)

Ingredients (1)

nateglinide (60 mg/1)

Linked Drug Pages (1)

Nateglinide ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "efa28dcf-77d5-4fb2-b6c0-4939a9bf4766", "openfda": {"nui": ["N0000175428", "N0000175448"], "unii": ["41X3PWK4O2"], "rxcui": ["311919", "314142"], "spl_set_id": ["c678b772-acba-4b59-a0b2-d70d84283425"], "pharm_class_epc": ["Glinide [EPC]"], "pharm_class_moa": ["Potassium Channel Antagonists [MoA]"], "manufacturer_name": ["Cadila Pharmaceuticals Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, COATED in 1 BOTTLE (71209-030-04)", "package_ndc": "71209-030-04", "marketing_start_date": "20201217"}, {"sample": false, "description": "100 TABLET, COATED in 1 BOTTLE (71209-030-05)", "package_ndc": "71209-030-05", "marketing_start_date": "20140210"}], "brand_name": "Nateglinide", "product_id": "71209-030_efa28dcf-77d5-4fb2-b6c0-4939a9bf4766", "dosage_form": "TABLET, COATED", "pharm_class": ["Glinide [EPC]", "Potassium Channel Antagonists [MoA]"], "product_ndc": "71209-030", "generic_name": "Nateglinide", "labeler_name": "Cadila Pharmaceuticals Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Nateglinide", "active_ingredients": [{"name": "NATEGLINIDE", "strength": "60 mg/1"}], "application_number": "ANDA206432", "marketing_category": "ANDA", "marketing_start_date": "20140210", "listing_expiration_date": "20261231"}