levothyroxine sodium
Generic: levothyroxine sodium
Labeler: a-s medication solutionsDrug Facts
Product Profile
Brand Name
levothyroxine sodium
Generic Name
levothyroxine sodium
Labeler
a-s medication solutions
Dosage Form
TABLET
Routes
Active Ingredients
levothyroxine sodium 125 ug/1
Manufacturer
Identifiers & Regulatory
Product NDC
50090-4799
Product ID
50090-4799_f2ee3fc5-4e2b-4b13-bd7c-7cbbf520ac1f
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
NDA
Application Number
NDA021116
Listing Expiration
2027-12-31
Marketing Start
2019-05-07
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
500904799
Hyphenated Format
50090-4799
Supplemental Identifiers
RxCUI
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
- 125 ug/1
Packaging
- 30 TABLET in 1 BOTTLE (50090-4799-0)
- 90 TABLET in 1 BOTTLE (50090-4799-1)
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "f2ee3fc5-4e2b-4b13-bd7c-7cbbf520ac1f", "openfda": {"unii": ["9J765S329G"], "rxcui": ["966224"], "spl_set_id": ["8f7dc71e-4a48-4ba5-945b-f340ff51636e"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (50090-4799-0)", "package_ndc": "50090-4799-0", "marketing_start_date": "20191216"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (50090-4799-1)", "package_ndc": "50090-4799-1", "marketing_start_date": "20191216"}], "brand_name": "levothyroxine sodium", "product_id": "50090-4799_f2ee3fc5-4e2b-4b13-bd7c-7cbbf520ac1f", "dosage_form": "TABLET", "pharm_class": ["Thyroxine [CS]", "l-Thyroxine [EPC]"], "product_ndc": "50090-4799", "generic_name": "levothyroxine sodium", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "levothyroxine sodium", "active_ingredients": [{"name": "LEVOTHYROXINE SODIUM", "strength": "125 ug/1"}], "application_number": "NDA021116", "marketing_category": "NDA", "marketing_start_date": "20190507", "listing_expiration_date": "20271231"}