levothyroxine sodium
Generic: levothyroxine sodium
Labeler: proficient rx lpDrug Facts
Product Profile
Brand Name
levothyroxine sodium
Generic Name
levothyroxine sodium
Labeler
proficient rx lp
Dosage Form
TABLET
Routes
Active Ingredients
levothyroxine sodium 25 ug/1
Manufacturer
Identifiers & Regulatory
Product NDC
82804-168
Product ID
82804-168_678b11e4-a8a5-4b9a-a937-517c9320372f
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA212399
Listing Expiration
2026-12-31
Marketing Start
2020-12-10
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
82804168
Hyphenated Format
82804-168
Supplemental Identifiers
RxCUI
UPC
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
ANDA212399 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 25 ug/1
Packaging
- 30 TABLET in 1 BOTTLE (82804-168-30)
- 90 TABLET in 1 BOTTLE (82804-168-90)
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "678b11e4-a8a5-4b9a-a937-517c9320372f", "openfda": {"upc": ["0382804168309"], "unii": ["9J765S329G"], "rxcui": ["966220"], "spl_set_id": ["576dcd01-d151-42ac-acd1-480a13bae176"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (82804-168-30)", "package_ndc": "82804-168-30", "marketing_start_date": "20241209"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (82804-168-90)", "package_ndc": "82804-168-90", "marketing_start_date": "20241223"}], "brand_name": "Levothyroxine sodium", "product_id": "82804-168_678b11e4-a8a5-4b9a-a937-517c9320372f", "dosage_form": "TABLET", "pharm_class": ["Thyroxine [CS]", "l-Thyroxine [EPC]"], "product_ndc": "82804-168", "generic_name": "Levothyroxine Sodium", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Levothyroxine sodium", "active_ingredients": [{"name": "LEVOTHYROXINE SODIUM", "strength": "25 ug/1"}], "application_number": "ANDA212399", "marketing_category": "ANDA", "marketing_start_date": "20201210", "listing_expiration_date": "20261231"}