levothyroxine sodium

Generic: levothyroxine sodium

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

Drug Facts

Product Profile

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

levothyroxine sodium 125 ug/1

Manufacturer
Teva Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 0480-8707
Product ID 0480-8707_8f65417f-488f-4e4a-894c-56f99ed57d25
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA207588
Marketing Start 2022-09-21
Marketing End 2026-04-30

Pharmacologic Class

Classes
thyroxine [cs] l-thyroxine [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 04808707
Hyphenated Format 0480-8707

Supplemental Identifiers

RxCUI
892246 892251 892255 966220 966221 966222 966224 966225 966248 966249 966253 966270
UPC
0304808704987 0304808725982 0304808690983 0304808718984 0304808715983 0304808682988 0304808693984
UNII
9J765S329G

Packaging Origin

Original Packager
true

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
  • 125 ug/1
source: ndc
Packaging
  • 1000 TABLET in 1 BOTTLE (0480-8707-10)
  • 90 TABLET in 1 BOTTLE (0480-8707-98)
source: ndc

Packages (2)

Ingredients (1)

levothyroxine sodium (125 ug/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "8f65417f-488f-4e4a-894c-56f99ed57d25", "openfda": {"upc": ["0304808704987", "0304808725982", "0304808690983", "0304808718984", "0304808715983", "0304808682988", "0304808693984"], "unii": ["9J765S329G"], "rxcui": ["892246", "892251", "892255", "966220", "966221", "966222", "966224", "966225", "966248", "966249", "966253", "966270"], "spl_set_id": ["60cadfd7-82b5-4207-97e1-1dd0655efb27"], "manufacturer_name": ["Teva Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET in 1 BOTTLE (0480-8707-10)", "package_ndc": "0480-8707-10", "marketing_end_date": "20260430", "marketing_start_date": "20220921"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (0480-8707-98)", "package_ndc": "0480-8707-98", "marketing_end_date": "20260430", "marketing_start_date": "20220921"}], "brand_name": "Levothyroxine sodium", "product_id": "0480-8707_8f65417f-488f-4e4a-894c-56f99ed57d25", "dosage_form": "TABLET", "pharm_class": ["Thyroxine [CS]", "l-Thyroxine [EPC]"], "product_ndc": "0480-8707", "generic_name": "Levothyroxine sodium", "labeler_name": "Teva Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Levothyroxine sodium", "active_ingredients": [{"name": "LEVOTHYROXINE SODIUM", "strength": "125 ug/1"}], "application_number": "ANDA207588", "marketing_category": "ANDA", "marketing_end_date": "20260430", "marketing_start_date": "20220921"}