levothyroxine sodium

Generic: levothyroxine sodium

Labeler: northwind health company, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name levothyroxine sodium
Generic Name levothyroxine sodium
Labeler northwind health company, llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

levothyroxine sodium 112 ug/1

Manufacturer
Northwind Health Company, LLC

Identifiers & Regulatory

Product NDC 51655-604
Product ID 51655-604_494f1d96-13bc-fa41-e063-6394a90a0912
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA076187
Listing Expiration 2027-12-31
Marketing Start 2021-02-18

Pharmacologic Class

Classes
thyroxine [cs] l-thyroxine [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 51655604
Hyphenated Format 51655-604

Supplemental Identifiers

RxCUI
966248
UNII
9J765S329G

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 ANDA076187 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 112 ug/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE, PLASTIC (51655-604-52)
source: ndc

Packages (1)

Ingredients (1)

levothyroxine sodium (112 ug/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "494f1d96-13bc-fa41-e063-6394a90a0912", "openfda": {"unii": ["9J765S329G"], "rxcui": ["966248"], "spl_set_id": ["db10e666-6204-56cc-e053-2995a90a9e08"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (51655-604-52)", "package_ndc": "51655-604-52", "marketing_start_date": "20210218"}], "brand_name": "Levothyroxine Sodium", "product_id": "51655-604_494f1d96-13bc-fa41-e063-6394a90a0912", "dosage_form": "TABLET", "pharm_class": ["Thyroxine [CS]", "l-Thyroxine [EPC]"], "product_ndc": "51655-604", "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": "112 ug/1"}], "application_number": "ANDA076187", "marketing_category": "ANDA", "marketing_start_date": "20210218", "listing_expiration_date": "20271231"}