levothyroxine sodium
Generic: levothyroxine sodium
Labeler: northwind health company, llcDrug Facts
Product Profile
Brand Name
levothyroxine sodium
Generic Name
levothyroxine sodium
Labeler
northwind health company, llc
Dosage Form
TABLET
Routes
Active Ingredients
levothyroxine sodium .137 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
51655-485
Product ID
51655-485_4a19de92-b6b6-9a77-e063-6394a90aae00
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA209713
Listing Expiration
2027-12-31
Marketing Start
2020-11-23
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
51655485
Hyphenated Format
51655-485
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, PLASTIC (51655-485-26)
- 30 TABLET in 1 BOTTLE, PLASTIC (51655-485-52)
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4a19de92-b6b6-9a77-e063-6394a90aae00", "openfda": {"unii": ["9J765S329G"], "rxcui": ["966270"], "spl_set_id": ["dac0af5d-622c-e18c-e053-2995a90a5739"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (51655-485-26)", "package_ndc": "51655-485-26", "marketing_start_date": "20201123"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (51655-485-52)", "package_ndc": "51655-485-52", "marketing_start_date": "20210420"}], "brand_name": "Levothyroxine Sodium", "product_id": "51655-485_4a19de92-b6b6-9a77-e063-6394a90aae00", "dosage_form": "TABLET", "pharm_class": ["Thyroxine [CS]", "l-Thyroxine [EPC]"], "product_ndc": "51655-485", "generic_name": "Levothyroxine Sodium", "labeler_name": "Northwind Health Company, LLC", "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": "20201123", "listing_expiration_date": "20271231"}