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 .137 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
50090-5792
Product ID
50090-5792_b0f7e2c1-8ff4-4405-96da-b93d1c63f1fe
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA209713
Listing Expiration
2026-12-31
Marketing Start
2019-03-20
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
500905792
Hyphenated Format
50090-5792
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
ANDA209713 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- .137 mg/1
Packaging
- 90 TABLET in 1 BOTTLE (50090-5792-0)
- 30 TABLET in 1 BOTTLE (50090-5792-1)
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "b0f7e2c1-8ff4-4405-96da-b93d1c63f1fe", "openfda": {"unii": ["9J765S329G"], "rxcui": ["966270"], "spl_set_id": ["924bb6e9-4b2b-406f-a0a8-376b1f22f1f5"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (50090-5792-0)", "package_ndc": "50090-5792-0", "marketing_start_date": "20211011"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (50090-5792-1)", "package_ndc": "50090-5792-1", "marketing_start_date": "20211011"}], "brand_name": "Levothyroxine Sodium", "product_id": "50090-5792_b0f7e2c1-8ff4-4405-96da-b93d1c63f1fe", "dosage_form": "TABLET", "pharm_class": ["Thyroxine [CS]", "l-Thyroxine [EPC]"], "product_ndc": "50090-5792", "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": ".137 mg/1"}], "application_number": "ANDA209713", "marketing_category": "ANDA", "marketing_start_date": "20190320", "listing_expiration_date": "20261231"}