levothyroxine sodium

Generic: levothyroxine sodium

Labeler: bryant ranch prepack
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name levothyroxine sodium
Generic Name levothyroxine sodium
Labeler bryant ranch prepack
Dosage Form TABLET
Routes
ORAL
Active Ingredients

levothyroxine sodium 50 ug/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 71335-1502
Product ID 71335-1502_5dd258ee-53fd-4e60-b3c9-b3cfacd622bf
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA021116
Listing Expiration 2026-12-31
Marketing Start 2019-05-07

Pharmacologic Class

Classes
thyroxine [cs] l-thyroxine [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 713351502
Hyphenated Format 71335-1502

Supplemental Identifiers

RxCUI
892246 892251 966220 966221 966222 966224 966225 966248 966249 966253 966270
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 NDA021116 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 ug/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (71335-1502-1)
  • 90 TABLET in 1 BOTTLE (71335-1502-2)
  • 100 TABLET in 1 BOTTLE (71335-1502-3)
  • 7 TABLET in 1 BOTTLE (71335-1502-4)
  • 14 TABLET in 1 BOTTLE (71335-1502-5)
  • 60 TABLET in 1 BOTTLE (71335-1502-6)
  • 21 TABLET in 1 BOTTLE (71335-1502-7)
  • 42 TABLET in 1 BOTTLE (71335-1502-8)
source: ndc

Packages (8)

71335-1502-1 30 TABLET in 1 BOTTLE (71335-1502-1) 71335-1502-2 90 TABLET in 1 BOTTLE (71335-1502-2) 71335-1502-3 100 TABLET in 1 BOTTLE (71335-1502-3) 71335-1502-4 7 TABLET in 1 BOTTLE (71335-1502-4) 71335-1502-5 14 TABLET in 1 BOTTLE (71335-1502-5) 71335-1502-6 60 TABLET in 1 BOTTLE (71335-1502-6) 71335-1502-7 21 TABLET in 1 BOTTLE (71335-1502-7) 71335-1502-8 42 TABLET in 1 BOTTLE (71335-1502-8)

Ingredients (1)

levothyroxine sodium (50 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": "5dd258ee-53fd-4e60-b3c9-b3cfacd622bf", "openfda": {"unii": ["9J765S329G"], "rxcui": ["892246", "892251", "966220", "966221", "966222", "966224", "966225", "966248", "966249", "966253", "966270"], "spl_set_id": ["9e3bffb9-f66e-4c73-befc-e60d769f6610"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (71335-1502-1)", "package_ndc": "71335-1502-1", "marketing_start_date": "20200224"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (71335-1502-2)", "package_ndc": "71335-1502-2", "marketing_start_date": "20240409"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (71335-1502-3)", "package_ndc": "71335-1502-3", "marketing_start_date": "20200224"}, {"sample": false, "description": "7 TABLET in 1 BOTTLE (71335-1502-4)", "package_ndc": "71335-1502-4", "marketing_start_date": "20200224"}, {"sample": false, "description": "14 TABLET in 1 BOTTLE (71335-1502-5)", "package_ndc": "71335-1502-5", "marketing_start_date": "20200224"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (71335-1502-6)", "package_ndc": "71335-1502-6", "marketing_start_date": "20200224"}, {"sample": false, "description": "21 TABLET in 1 BOTTLE (71335-1502-7)", "package_ndc": "71335-1502-7", "marketing_start_date": "20200224"}, {"sample": false, "description": "42 TABLET in 1 BOTTLE (71335-1502-8)", "package_ndc": "71335-1502-8", "marketing_start_date": "20200224"}], "brand_name": "levothyroxine sodium", "product_id": "71335-1502_5dd258ee-53fd-4e60-b3c9-b3cfacd622bf", "dosage_form": "TABLET", "pharm_class": ["Thyroxine [CS]", "l-Thyroxine [EPC]"], "product_ndc": "71335-1502", "generic_name": "levothyroxine sodium", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "levothyroxine sodium", "active_ingredients": [{"name": "LEVOTHYROXINE SODIUM", "strength": "50 ug/1"}], "application_number": "NDA021116", "marketing_category": "NDA", "marketing_start_date": "20190507", "listing_expiration_date": "20261231"}