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 ug/1
Manufacturer
Identifiers & Regulatory
Product NDC
50090-7801
Product ID
50090-7801_5fedb1b2-55c6-4e69-a8ed-b1d2b5ecff60
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA211417
Listing Expiration
2026-12-31
Marketing Start
2025-04-08
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
500907801
Hyphenated Format
50090-7801
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
ANDA211417 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 137 ug/1
Packaging
- 90 TABLET in 1 BOTTLE (50090-7801-0)
- 30 TABLET in 1 BOTTLE (50090-7801-1)
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "5fedb1b2-55c6-4e69-a8ed-b1d2b5ecff60", "openfda": {"unii": ["9J765S329G"], "rxcui": ["966270"], "spl_set_id": ["2adb05ef-b3fa-4ac2-b219-99442746392b"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (50090-7801-0)", "package_ndc": "50090-7801-0", "marketing_start_date": "20251201"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (50090-7801-1)", "package_ndc": "50090-7801-1", "marketing_start_date": "20251201"}], "brand_name": "LEVOTHYROXINE SODIUM", "product_id": "50090-7801_5fedb1b2-55c6-4e69-a8ed-b1d2b5ecff60", "dosage_form": "TABLET", "pharm_class": ["Thyroxine [CS]", "l-Thyroxine [EPC]"], "product_ndc": "50090-7801", "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 ug/1"}], "application_number": "ANDA211417", "marketing_category": "ANDA", "marketing_start_date": "20250408", "listing_expiration_date": "20261231"}