levothyroxine sodium

Generic: levothyroxine sodium

Labeler: preferred pharmaceuticals inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name levothyroxine sodium
Generic Name levothyroxine sodium
Labeler preferred pharmaceuticals inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

levothyroxine sodium 200 ug/1

Manufacturer
Preferred Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 68788-8902
Product ID 68788-8902_64aaeba7-1013-44a4-96fc-b876016897b3
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA207588
Listing Expiration 2026-12-31
Marketing Start 2025-07-25

Pharmacologic Class

Classes
thyroxine [cs] l-thyroxine [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 687888902
Hyphenated Format 68788-8902

Supplemental Identifiers

RxCUI
892251
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 ANDA207588 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 200 ug/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (68788-8902-3)
  • 90 TABLET in 1 BOTTLE (68788-8902-9)
source: ndc

Packages (2)

68788-8902-3 30 TABLET in 1 BOTTLE (68788-8902-3) 68788-8902-9 90 TABLET in 1 BOTTLE (68788-8902-9)

Ingredients (1)

levothyroxine sodium (200 ug/1)

Linked Drug Pages (1)

Levothyroxine sodium ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "64aaeba7-1013-44a4-96fc-b876016897b3", "openfda": {"unii": ["9J765S329G"], "rxcui": ["892251"], "spl_set_id": ["64aaeba7-1013-44a4-96fc-b876016897b3"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (68788-8902-3)", "package_ndc": "68788-8902-3", "marketing_start_date": "20250725"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (68788-8902-9)", "package_ndc": "68788-8902-9", "marketing_start_date": "20250725"}], "brand_name": "Levothyroxine sodium", "product_id": "68788-8902_64aaeba7-1013-44a4-96fc-b876016897b3", "dosage_form": "TABLET", "pharm_class": ["Thyroxine [CS]", "l-Thyroxine [EPC]"], "product_ndc": "68788-8902", "generic_name": "Levothyroxine sodium", "labeler_name": "Preferred Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Levothyroxine sodium", "active_ingredients": [{"name": "LEVOTHYROXINE SODIUM", "strength": "200 ug/1"}], "application_number": "ANDA207588", "marketing_category": "ANDA", "marketing_start_date": "20250725", "listing_expiration_date": "20261231"}