levothyroxine sodium

Generic: levothyroxine sodium

Labeler: nucar pharmaceuticals,inc.
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

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

levothyroxine sodium 100 ug/1

Manufacturer
NuCar Pharmaceuticals,Inc.

Identifiers & Regulatory

Product NDC 68071-5235
Product ID 68071-5235_1b593159-b796-10ad-e063-6294a90abd25
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA021116
Listing Expiration 2026-12-31
Marketing Start 2019-05-07

Pharmacologic Class

Classes
thyroxine [cs] l-thyroxine [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 680715235
Hyphenated Format 68071-5235

Supplemental Identifiers

RxCUI
892246
UPC
0368071523591
UNII
9J765S329G

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 levothyroxine sodium (source: ndc)
Generic Name levothyroxine sodium (source: ndc)
Application Number NDA021116 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 100 ug/1
source: ndc
Packaging
  • 90 TABLET in 1 BOTTLE (68071-5235-9)
source: ndc

Packages (1)

68071-5235-9 90 TABLET in 1 BOTTLE (68071-5235-9)

Ingredients (1)

levothyroxine sodium (100 ug/1)

Linked Drug Pages (1)

levothyroxine sodium ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "1b593159-b796-10ad-e063-6294a90abd25", "openfda": {"upc": ["0368071523591"], "unii": ["9J765S329G"], "rxcui": ["892246"], "spl_set_id": ["a2194c58-b755-e6b5-e053-2a95a90a36d4"], "manufacturer_name": ["NuCar Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (68071-5235-9)", "package_ndc": "68071-5235-9", "marketing_start_date": "20200330"}], "brand_name": "levothyroxine sodium", "product_id": "68071-5235_1b593159-b796-10ad-e063-6294a90abd25", "dosage_form": "TABLET", "pharm_class": ["Thyroxine [CS]", "l-Thyroxine [EPC]"], "product_ndc": "68071-5235", "generic_name": "levothyroxine sodium", "labeler_name": "NuCar Pharmaceuticals,Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "levothyroxine sodium", "active_ingredients": [{"name": "LEVOTHYROXINE SODIUM", "strength": "100 ug/1"}], "application_number": "NDA021116", "marketing_category": "NDA", "marketing_start_date": "20190507", "listing_expiration_date": "20261231"}