levothyroxine sodium

Generic: levothyroxine sodium

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

Drug Facts

Product Profile

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

levothyroxine sodium 75 ug/1

Manufacturer
NuCare Pharmaceuticals,Inc.

Identifiers & Regulatory

Product NDC 68071-5227
Product ID 68071-5227_1b592020-c769-2381-e063-6394a90a74b7
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 680715227
Hyphenated Format 68071-5227

Supplemental Identifiers

RxCUI
966222
UPC
0368071522792
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
  • 75 ug/1
source: ndc
Packaging
  • 90 TABLET in 1 BOTTLE (68071-5227-9)
source: ndc

Packages (1)

Ingredients (1)

levothyroxine sodium (75 ug/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "1b592020-c769-2381-e063-6394a90a74b7", "openfda": {"upc": ["0368071522792"], "unii": ["9J765S329G"], "rxcui": ["966222"], "spl_set_id": ["a215da96-acd9-6b8d-e053-2995a90a7e0d"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (68071-5227-9)", "package_ndc": "68071-5227-9", "marketing_start_date": "20200330"}], "brand_name": "levothyroxine sodium", "product_id": "68071-5227_1b592020-c769-2381-e063-6394a90a74b7", "dosage_form": "TABLET", "pharm_class": ["Thyroxine [CS]", "l-Thyroxine [EPC]"], "product_ndc": "68071-5227", "generic_name": "levothyroxine sodium", "labeler_name": "NuCare Pharmaceuticals,Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "levothyroxine sodium", "active_ingredients": [{"name": "LEVOTHYROXINE SODIUM", "strength": "75 ug/1"}], "application_number": "NDA021116", "marketing_category": "NDA", "marketing_start_date": "20190507", "listing_expiration_date": "20261231"}