levothyroxine sodium

Generic: levothyroxine sodium

Labeler: nucare pharmaceuticals,inc.
NDC Directory HUMAN PRESCRIPTION DRUG NDA AUTHORIZED GENERIC 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 100 ug/1

Manufacturer
NuCare Pharmaceuticals,Inc.

Identifiers & Regulatory

Product NDC 68071-2278
Product ID 68071-2278_1d7815c7-abd3-9fbd-e063-6394a90a11f7
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA AUTHORIZED GENERIC
Application Number NDA021342
Listing Expiration 2026-12-31
Marketing Start 2020-08-03

Pharmacologic Class

Classes
thyroxine [cs] l-thyroxine [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 680712278
Hyphenated Format 68071-2278

Supplemental Identifiers

RxCUI
892246
UPC
0368071227895
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 NDA021342 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 100 ug/1
source: ndc
Packaging
  • 90 TABLET in 1 BOTTLE (68071-2278-9)
source: ndc

Packages (1)

68071-2278-9 90 TABLET in 1 BOTTLE (68071-2278-9)

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": "1d7815c7-abd3-9fbd-e063-6394a90a11f7", "openfda": {"upc": ["0368071227895"], "unii": ["9J765S329G"], "rxcui": ["892246"], "spl_set_id": ["b1b8c5a4-8132-24d2-e053-2995a90a59ec"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (68071-2278-9)", "package_ndc": "68071-2278-9", "marketing_start_date": "20201015"}], "brand_name": "Levothyroxine Sodium", "product_id": "68071-2278_1d7815c7-abd3-9fbd-e063-6394a90a11f7", "dosage_form": "TABLET", "pharm_class": ["Thyroxine [CS]", "l-Thyroxine [EPC]"], "product_ndc": "68071-2278", "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": "100 ug/1"}], "application_number": "NDA021342", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20200803", "listing_expiration_date": "20261231"}