nateglinide

Generic: nateglinide

Labeler: american health packaging
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name nateglinide
Generic Name nateglinide
Labeler american health packaging
Dosage Form TABLET
Routes
ORAL
Active Ingredients

nateglinide 120 mg/1

Manufacturer
American Health Packaging

Identifiers & Regulatory

Product NDC 60687-684
Product ID 60687-684_2b2511ab-0768-113f-e063-6394a90a809d
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA077463
Listing Expiration 2026-12-31
Marketing Start 2023-01-03

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 60687684
Hyphenated Format 60687-684

Supplemental Identifiers

RxCUI
311919 314142
UNII
41X3PWK4O2
NUI
N0000175428 N0000175448

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 ANDA077463 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 120 mg/1
source: ndc
Packaging
  • 30 BLISTER PACK in 1 CARTON (60687-684-21) / 1 TABLET in 1 BLISTER PACK (60687-684-11)
source: ndc

Packages (1)

60687-684-21 30 BLISTER PACK in 1 CARTON (60687-684-21) / 1 TABLET in 1 BLISTER PACK (60687-684-11)

Ingredients (1)

nateglinide (120 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": "2b2511ab-0768-113f-e063-6394a90a809d", "openfda": {"nui": ["N0000175428", "N0000175448"], "unii": ["41X3PWK4O2"], "rxcui": ["311919", "314142"], "spl_set_id": ["b17ead66-dc11-4e54-9ba6-00619510f27b"], "pharm_class_epc": ["Glinide [EPC]"], "pharm_class_moa": ["Potassium Channel Antagonists [MoA]"], "manufacturer_name": ["American Health Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "30 BLISTER PACK in 1 CARTON (60687-684-21)  / 1 TABLET in 1 BLISTER PACK (60687-684-11)", "package_ndc": "60687-684-21", "marketing_start_date": "20230103"}], "brand_name": "Nateglinide", "product_id": "60687-684_2b2511ab-0768-113f-e063-6394a90a809d", "dosage_form": "TABLET", "pharm_class": ["Glinide [EPC]", "Potassium Channel Antagonists [MoA]"], "product_ndc": "60687-684", "generic_name": "nateglinide", "labeler_name": "American Health Packaging", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Nateglinide", "active_ingredients": [{"name": "NATEGLINIDE", "strength": "120 mg/1"}], "application_number": "ANDA077463", "marketing_category": "ANDA", "marketing_start_date": "20230103", "listing_expiration_date": "20261231"}