levothyroxine sodium

Generic: levothyroxine sodium

Labeler: northstar rxllc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name levothyroxine sodium
Generic Name levothyroxine sodium
Labeler northstar rxllc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

levothyroxine sodium 88 ug/1

Manufacturer
NorthStar RxLLC

Identifiers & Regulatory

Product NDC 72603-663
Product ID 72603-663_e51d8ca0-2d22-4390-ba97-f0075e7cc256
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA211417
Listing Expiration 2026-12-31
Marketing Start 2025-04-08

Pharmacologic Class

Classes
thyroxine [cs] l-thyroxine [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72603663
Hyphenated Format 72603-663

Supplemental Identifiers

RxCUI
892246 892251 966220 966221 966222 966224 966225 966248 966249 966253 966270
UPC
0372603667011 0372603665017
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 ANDA211417 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 88 ug/1
source: ndc
Packaging
  • 1000 TABLET in 1 BOTTLE (72603-663-01)
source: ndc

Packages (1)

72603-663-01 1000 TABLET in 1 BOTTLE (72603-663-01)

Ingredients (1)

levothyroxine sodium (88 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": "e51d8ca0-2d22-4390-ba97-f0075e7cc256", "openfda": {"upc": ["0372603667011", "0372603665017"], "unii": ["9J765S329G"], "rxcui": ["892246", "892251", "966220", "966221", "966222", "966224", "966225", "966248", "966249", "966253", "966270"], "spl_set_id": ["58f4dc90-3648-49dc-a7e1-baf918a773b5"], "manufacturer_name": ["NorthStar RxLLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET in 1 BOTTLE (72603-663-01)", "package_ndc": "72603-663-01", "marketing_start_date": "20250408"}], "brand_name": "LEVOTHYROXINE SODIUM", "product_id": "72603-663_e51d8ca0-2d22-4390-ba97-f0075e7cc256", "dosage_form": "TABLET", "pharm_class": ["Thyroxine [CS]", "l-Thyroxine [EPC]"], "product_ndc": "72603-663", "generic_name": "LEVOTHYROXINE SODIUM", "labeler_name": "NorthStar RxLLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "LEVOTHYROXINE SODIUM", "active_ingredients": [{"name": "LEVOTHYROXINE SODIUM", "strength": "88 ug/1"}], "application_number": "ANDA211417", "marketing_category": "ANDA", "marketing_start_date": "20250408", "listing_expiration_date": "20261231"}