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 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
50090-6982
Product ID
50090-6982_48fee4f7-f275-45cf-8d4e-ad207cf91b23
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA209713
Listing Expiration
2027-12-31
Marketing Start
2019-03-20
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
500906982
Hyphenated Format
50090-6982
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
- .125 mg/1
Packaging
- 30 TABLET in 1 BOTTLE (50090-6982-0)
- 90 TABLET in 1 BOTTLE (50090-6982-1)
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "48fee4f7-f275-45cf-8d4e-ad207cf91b23", "openfda": {"unii": ["9J765S329G"], "rxcui": ["966224"], "spl_set_id": ["e2291336-1188-48f4-af52-d12ac892f80f"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (50090-6982-0)", "package_ndc": "50090-6982-0", "marketing_start_date": "20231226"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (50090-6982-1)", "package_ndc": "50090-6982-1", "marketing_start_date": "20231226"}], "brand_name": "Levothyroxine Sodium", "product_id": "50090-6982_48fee4f7-f275-45cf-8d4e-ad207cf91b23", "dosage_form": "TABLET", "pharm_class": ["Thyroxine [CS]", "l-Thyroxine [EPC]"], "product_ndc": "50090-6982", "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 mg/1"}], "application_number": "ANDA209713", "marketing_category": "ANDA", "marketing_start_date": "20190320", "listing_expiration_date": "20271231"}