repaglinide

Generic: repaglinide

Labeler: northstar rxllc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name repaglinide
Generic Name repaglinide
Labeler northstar rxllc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

repaglinide 1 mg/1

Manufacturer
NorthStar RxLLC

Identifiers & Regulatory

Product NDC 72603-811
Product ID 72603-811_19426809-2230-4ebf-a29a-40e25326a943
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA207209
Listing Expiration 2026-12-31
Marketing Start 2025-04-08

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 72603811
Hyphenated Format 72603-811

Supplemental Identifiers

RxCUI
200256 200257 200258
UPC
0372603812015 0372603811018 0372603810011
UNII
668Z8C33LU
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 repaglinide (source: ndc)
Generic Name repaglinide (source: ndc)
Application Number ANDA207209 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (72603-811-01)
source: ndc

Packages (1)

72603-811-01 100 TABLET in 1 BOTTLE (72603-811-01)

Ingredients (1)

repaglinide (1 mg/1)

Linked Drug Pages (1)

Repaglinide ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "19426809-2230-4ebf-a29a-40e25326a943", "openfda": {"nui": ["N0000175428", "N0000175448"], "upc": ["0372603812015", "0372603811018", "0372603810011"], "unii": ["668Z8C33LU"], "rxcui": ["200256", "200257", "200258"], "spl_set_id": ["7f3118ce-fcbb-4f8b-b1ba-d8cd95e5b665"], "pharm_class_epc": ["Glinide [EPC]"], "pharm_class_moa": ["Potassium Channel Antagonists [MoA]"], "manufacturer_name": ["NorthStar RxLLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (72603-811-01)", "package_ndc": "72603-811-01", "marketing_start_date": "20250408"}], "brand_name": "Repaglinide", "product_id": "72603-811_19426809-2230-4ebf-a29a-40e25326a943", "dosage_form": "TABLET", "pharm_class": ["Glinide [EPC]", "Potassium Channel Antagonists [MoA]"], "product_ndc": "72603-811", "generic_name": "Repaglinide", "labeler_name": "NorthStar RxLLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Repaglinide", "active_ingredients": [{"name": "REPAGLINIDE", "strength": "1 mg/1"}], "application_number": "ANDA207209", "marketing_category": "ANDA", "marketing_start_date": "20250408", "listing_expiration_date": "20261231"}