levothyroxine sodium

Generic: levothyroxine sodium

Labeler: alvogen, inc.
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

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

levothyroxine sodium 150 ug/1

Manufacturer
Alvogen, Inc.

Identifiers & Regulatory

Product NDC 47781-662
Product ID 47781-662_12e236b4-dc71-96ce-cdd3-7bede41b3f1c
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 47781662
Hyphenated Format 47781-662

Supplemental Identifiers

RxCUI
892246 892251 892255 966220 966221 966222 966224 966225 966248 966249 966253 966270
UPC
0347781649906 0347781671907 0347781643904 0347781657901 0347781640903 0347781651909 0347781662905 0347781665906 0347781646905 0347781654900 0347781659905
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 NDA021116 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 150 ug/1
source: ndc
Packaging
  • 1000 TABLET in 1 BOTTLE (47781-662-10)
  • 90 TABLET in 1 BOTTLE (47781-662-90)
source: ndc

Packages (2)

47781-662-10 1000 TABLET in 1 BOTTLE (47781-662-10) 47781-662-90 90 TABLET in 1 BOTTLE (47781-662-90)

Ingredients (1)

levothyroxine sodium (150 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": "12e236b4-dc71-96ce-cdd3-7bede41b3f1c", "openfda": {"upc": ["0347781649906", "0347781671907", "0347781643904", "0347781657901", "0347781640903", "0347781651909", "0347781662905", "0347781665906", "0347781646905", "0347781654900", "0347781659905"], "unii": ["9J765S329G"], "rxcui": ["892246", "892251", "892255", "966220", "966221", "966222", "966224", "966225", "966248", "966249", "966253", "966270"], "spl_set_id": ["4ddcaec1-a58f-340b-9bc1-bbe048b8c885"], "manufacturer_name": ["Alvogen, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET in 1 BOTTLE (47781-662-10)", "package_ndc": "47781-662-10", "marketing_start_date": "20190507"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (47781-662-90)", "package_ndc": "47781-662-90", "marketing_start_date": "20190507"}], "brand_name": "levothyroxine sodium", "product_id": "47781-662_12e236b4-dc71-96ce-cdd3-7bede41b3f1c", "dosage_form": "TABLET", "pharm_class": ["Thyroxine [CS]", "l-Thyroxine [EPC]"], "product_ndc": "47781-662", "generic_name": "levothyroxine sodium", "labeler_name": "Alvogen, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "levothyroxine sodium", "active_ingredients": [{"name": "LEVOTHYROXINE SODIUM", "strength": "150 ug/1"}], "application_number": "NDA021116", "marketing_category": "NDA", "marketing_start_date": "20190507", "listing_expiration_date": "20261231"}