levothyroxine sodium
Generic: levothyroxine sodium
Labeler: direct rxDrug Facts
Product Profile
Brand Name
levothyroxine sodium
Generic Name
levothyroxine sodium
Labeler
direct rx
Dosage Form
TABLET
Routes
Active Ingredients
levothyroxine sodium 112 ug/1
Manufacturer
Identifiers & Regulatory
Product NDC
72189-159
Product ID
72189-159_1922dbd9-96de-8652-e063-6294a90a0afe
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
NDA
Application Number
NDA021116
Listing Expiration
2026-12-31
Marketing Start
2020-12-01
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
72189159
Hyphenated Format
72189-159
Supplemental Identifiers
RxCUI
UNII
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
source: ndc
Resolved Composition
Strengths
- 112 ug/1
Packaging
- 30 TABLET in 1 BOTTLE (72189-159-30)
- 90 TABLET in 1 BOTTLE (72189-159-90)
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "1922dbd9-96de-8652-e063-6294a90a0afe", "openfda": {"unii": ["9J765S329G"], "rxcui": ["892246", "966220", "966221", "966222", "966224", "966225", "966248", "966253", "966270"], "spl_set_id": ["a5f15022-1166-09fe-e053-2a95a90aa218"], "manufacturer_name": ["DIRECT RX"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (72189-159-30)", "package_ndc": "72189-159-30", "marketing_start_date": "20201201"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (72189-159-90)", "package_ndc": "72189-159-90", "marketing_start_date": "20201201"}], "brand_name": "LEVOTHYROXINE SODIUM", "product_id": "72189-159_1922dbd9-96de-8652-e063-6294a90a0afe", "dosage_form": "TABLET", "pharm_class": ["Thyroxine [CS]", "l-Thyroxine [EPC]"], "product_ndc": "72189-159", "generic_name": "LEVOTHYROXINE SODIUM", "labeler_name": "DIRECT RX", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "LEVOTHYROXINE SODIUM", "active_ingredients": [{"name": "LEVOTHYROXINE SODIUM", "strength": "112 ug/1"}], "application_number": "NDA021116", "marketing_category": "NDA", "marketing_start_date": "20201201", "listing_expiration_date": "20261231"}