levothyroxine sodium
Generic: levothyroxine sodium
Labeler: preferred pharmaceuticals inc.Drug Facts
Product Profile
Brand Name
levothyroxine sodium
Generic Name
levothyroxine sodium
Labeler
preferred pharmaceuticals inc.
Dosage Form
TABLET
Routes
Active Ingredients
levothyroxine sodium 25 ug/1
Manufacturer
Identifiers & Regulatory
Product NDC
68788-7969
Product ID
68788-7969_cac8cf0b-89b2-43dd-80cb-ede3eba51281
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA212399
Listing Expiration
2026-12-31
Marketing Start
2021-07-28
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
687887969
Hyphenated Format
68788-7969
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
ANDA212399 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 25 ug/1
Packaging
- 30 TABLET in 1 BOTTLE (68788-7969-3)
- 90 TABLET in 1 BOTTLE (68788-7969-9)
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "cac8cf0b-89b2-43dd-80cb-ede3eba51281", "openfda": {"unii": ["9J765S329G"], "rxcui": ["966220"], "spl_set_id": ["633b3f9c-9578-4e07-a515-aec1a8b65e92"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (68788-7969-3)", "package_ndc": "68788-7969-3", "marketing_start_date": "20210728"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (68788-7969-9)", "package_ndc": "68788-7969-9", "marketing_start_date": "20210728"}], "brand_name": "Levothyroxine sodium", "product_id": "68788-7969_cac8cf0b-89b2-43dd-80cb-ede3eba51281", "dosage_form": "TABLET", "pharm_class": ["Thyroxine [CS]", "l-Thyroxine [EPC]"], "product_ndc": "68788-7969", "generic_name": "Levothyroxine Sodium", "labeler_name": "Preferred Pharmaceuticals Inc.", "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": "20210728", "listing_expiration_date": "20261231"}