liothyronine sodium

Generic: liothyronine sodium

Labeler: sun pharmaceutical industries, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name liothyronine sodium
Generic Name liothyronine sodium
Labeler sun pharmaceutical industries, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

liothyronine sodium 50 ug/1

Manufacturer
Sun Pharmaceutical Industries, Inc.

Identifiers & Regulatory

Product NDC 62756-591
Product ID 62756-591_af12cd5c-3963-4ef2-b819-a42343f0cb69
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA091382
Listing Expiration 2026-12-31
Marketing Start 2019-11-28

Pharmacologic Class

Classes
triiodothyronine [cs] l-triiodothyronine [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 62756591
Hyphenated Format 62756-591

Supplemental Identifiers

RxCUI
903456 903697 903703
UNII
GCA9VV7D2N

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 liothyronine sodium (source: ndc)
Generic Name liothyronine sodium (source: ndc)
Application Number ANDA091382 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 ug/1
source: ndc
Packaging
  • 90 TABLET in 1 BOTTLE (62756-591-01)
  • 100 TABLET in 1 BOTTLE (62756-591-08)
  • 1000 TABLET in 1 BOTTLE (62756-591-18)
  • 30 TABLET in 1 BOTTLE (62756-591-83)
  • 100 TABLET in 1 BOTTLE (62756-591-88)
source: ndc

Packages (5)

62756-591-01 90 TABLET in 1 BOTTLE (62756-591-01) 62756-591-08 100 TABLET in 1 BOTTLE (62756-591-08) 62756-591-18 1000 TABLET in 1 BOTTLE (62756-591-18) 62756-591-83 30 TABLET in 1 BOTTLE (62756-591-83) 62756-591-88 100 TABLET in 1 BOTTLE (62756-591-88)

Ingredients (1)

liothyronine sodium (50 ug/1)

Linked Drug Pages (1)

liothyronine sodium ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "af12cd5c-3963-4ef2-b819-a42343f0cb69", "openfda": {"unii": ["GCA9VV7D2N"], "rxcui": ["903456", "903697", "903703"], "spl_set_id": ["892e63ef-3a60-45fa-b12b-d6795acc0956"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (62756-591-01)", "package_ndc": "62756-591-01", "marketing_start_date": "20230626"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (62756-591-08)", "package_ndc": "62756-591-08", "marketing_start_date": "20191128"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (62756-591-18)", "package_ndc": "62756-591-18", "marketing_start_date": "20191128"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (62756-591-83)", "package_ndc": "62756-591-83", "marketing_start_date": "20191128"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (62756-591-88)", "package_ndc": "62756-591-88", "marketing_start_date": "20191128"}], "brand_name": "liothyronine sodium", "product_id": "62756-591_af12cd5c-3963-4ef2-b819-a42343f0cb69", "dosage_form": "TABLET", "pharm_class": ["Triiodothyronine [CS]", "l-Triiodothyronine [EPC]"], "product_ndc": "62756-591", "generic_name": "liothyronine sodium", "labeler_name": "Sun Pharmaceutical Industries, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "liothyronine sodium", "active_ingredients": [{"name": "LIOTHYRONINE SODIUM", "strength": "50 ug/1"}], "application_number": "ANDA091382", "marketing_category": "ANDA", "marketing_start_date": "20191128", "listing_expiration_date": "20261231"}