liothyronine sodium

Generic: liothyronine sodium

Labeler: nucare pharmaceuticals,inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name liothyronine sodium
Generic Name liothyronine sodium
Labeler nucare pharmaceuticals,inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

liothyronine sodium 5 ug/1

Manufacturer
NuCare Pharmaceuticals,Inc.

Identifiers & Regulatory

Product NDC 68071-3571
Product ID 68071-3571_1133ebe8-38c3-2505-e063-6294a90aaa2f
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA200295
Listing Expiration 2026-12-31
Marketing Start 2012-12-03

Pharmacologic Class

Classes
triiodothyronine [cs] l-triiodothyronine [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 680713571
Hyphenated Format 68071-3571

Supplemental Identifiers

RxCUI
903456
UPC
0368071357196
UNII
GCA9VV7D2N

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 ANDA200295 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 5 ug/1
source: ndc
Packaging
  • 90 TABLET in 1 BOTTLE (68071-3571-9)
source: ndc

Packages (1)

Ingredients (1)

liothyronine sodium (5 ug/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "1133ebe8-38c3-2505-e063-6294a90aaa2f", "openfda": {"upc": ["0368071357196"], "unii": ["GCA9VV7D2N"], "rxcui": ["903456"], "spl_set_id": ["1133ebe8-38c2-2505-e063-6294a90aaa2f"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (68071-3571-9)", "package_ndc": "68071-3571-9", "marketing_start_date": "20240212"}], "brand_name": "Liothyronine Sodium", "product_id": "68071-3571_1133ebe8-38c3-2505-e063-6294a90aaa2f", "dosage_form": "TABLET", "pharm_class": ["Triiodothyronine [CS]", "l-Triiodothyronine [EPC]"], "product_ndc": "68071-3571", "generic_name": "Liothyronine Sodium", "labeler_name": "NuCare Pharmaceuticals,Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Liothyronine Sodium", "active_ingredients": [{"name": "LIOTHYRONINE SODIUM", "strength": "5 ug/1"}], "application_number": "ANDA200295", "marketing_category": "ANDA", "marketing_start_date": "20121203", "listing_expiration_date": "20261231"}