levothyroxine sodium
Generic: levothyroxine sodium
Labeler: nucare pharmaceuticals,inc.Drug Facts
Product Profile
Brand Name
levothyroxine sodium
Generic Name
levothyroxine sodium
Labeler
nucare pharmaceuticals,inc.
Dosage Form
TABLET
Routes
Active Ingredients
levothyroxine sodium 75 ug/1
Manufacturer
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
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
680715227
Hyphenated Format
68071-5227
Supplemental Identifiers
RxCUI
UPC
UNII
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
source: ndc
Resolved Composition
Strengths
- 75 ug/1
Packaging
- 90 TABLET in 1 BOTTLE (68071-5227-9)
Packages (1)
Ingredients (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"}