synthroid

Generic: levothyroxine sodium

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

Drug Facts

Product Profile

Brand Name synthroid
Generic Name levothyroxine sodium
Labeler abbvie inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

levothyroxine sodium 50 ug/1

Manufacturer
AbbVie Inc.

Identifiers & Regulatory

Product NDC 0074-4552
Product ID 0074-4552_b85ab7fa-ba96-43cd-b736-44b3924e644c
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA021402
Listing Expiration 2026-12-31
Marketing Start 2002-07-24

Pharmacologic Class

Classes
thyroxine [cs] l-thyroxine [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 00744552
Hyphenated Format 0074-4552

Supplemental Identifiers

RxCUI
892246 892251 892255 966158 966171 966185 966191 966201 966205 966218 966220 966221 966222 966224 966225 966247 966248 966249 966250 966251 966253 966270 966271 966282
UPC
0300747149902 0300747068197 0300744341194 0300745182192 0300747070190 0300747069903 0300749296192 0300743727906 0300747148905 0300746624905
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 synthroid (source: ndc)
Generic Name levothyroxine sodium (source: ndc)
Application Number NDA021402 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 ug/1
source: ndc
Packaging
  • 10 BLISTER PACK in 1 BOX, UNIT-DOSE (0074-4552-11) / 10 TABLET in 1 BLISTER PACK
  • 1000 TABLET in 1 BOTTLE (0074-4552-19)
  • 2 BLISTER PACK in 1 CARTON (0074-4552-72) / 7 TABLET in 1 BLISTER PACK
  • 90 TABLET in 1 BOTTLE (0074-4552-90)
source: ndc

Packages (4)

0074-4552-11 10 BLISTER PACK in 1 BOX, UNIT-DOSE (0074-4552-11) / 10 TABLET in 1 BLISTER PACK 0074-4552-19 1000 TABLET in 1 BOTTLE (0074-4552-19) 0074-4552-72 2 BLISTER PACK in 1 CARTON (0074-4552-72) / 7 TABLET in 1 BLISTER PACK 0074-4552-90 90 TABLET in 1 BOTTLE (0074-4552-90)

Ingredients (1)

levothyroxine sodium (50 ug/1)

Linked Drug Pages (1)

Synthroid ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "b85ab7fa-ba96-43cd-b736-44b3924e644c", "openfda": {"upc": ["0300747149902", "0300747068197", "0300744341194", "0300745182192", "0300747070190", "0300747069903", "0300749296192", "0300743727906", "0300747148905", "0300746624905"], "unii": ["9J765S329G"], "rxcui": ["892246", "892251", "892255", "966158", "966171", "966185", "966191", "966201", "966205", "966218", "966220", "966221", "966222", "966224", "966225", "966247", "966248", "966249", "966250", "966251", "966253", "966270", "966271", "966282"], "spl_set_id": ["1e11ad30-1041-4520-10b0-8f9d30d30fcc"], "manufacturer_name": ["AbbVie Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 BLISTER PACK in 1 BOX, UNIT-DOSE (0074-4552-11)  / 10 TABLET in 1 BLISTER PACK", "package_ndc": "0074-4552-11", "marketing_start_date": "20020724"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (0074-4552-19)", "package_ndc": "0074-4552-19", "marketing_start_date": "20020724"}, {"sample": true, "description": "2 BLISTER PACK in 1 CARTON (0074-4552-72)  / 7 TABLET in 1 BLISTER PACK", "package_ndc": "0074-4552-72", "marketing_start_date": "20020724"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (0074-4552-90)", "package_ndc": "0074-4552-90", "marketing_start_date": "20020724"}], "brand_name": "Synthroid", "product_id": "0074-4552_b85ab7fa-ba96-43cd-b736-44b3924e644c", "dosage_form": "TABLET", "pharm_class": ["Thyroxine [CS]", "l-Thyroxine [EPC]"], "product_ndc": "0074-4552", "generic_name": "Levothyroxine Sodium", "labeler_name": "AbbVie Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Synthroid", "active_ingredients": [{"name": "LEVOTHYROXINE SODIUM", "strength": "50 ug/1"}], "application_number": "NDA021402", "marketing_category": "NDA", "marketing_start_date": "20020724", "listing_expiration_date": "20261231"}