levothyroxine sodium

Generic: levothyroxine sodium

Labeler: nucare pharmaceuticals,inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name levothyroxine sodium
Generic Name levothyroxine sodium
Labeler nucare pharmaceuticals,inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

levothyroxine sodium 200 ug/1

Manufacturer
NuCare Pharmaceuticals,Inc.

Identifiers & Regulatory

Product NDC 68071-3619
Product ID 68071-3619_1ac85666-6200-3887-e063-6394a90a105e
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA212399
Listing Expiration 2026-12-31
Marketing Start 2020-12-03

Pharmacologic Class

Classes
thyroxine [cs] l-thyroxine [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 680713619
Hyphenated Format 68071-3619

Supplemental Identifiers

RxCUI
892251
UPC
0368071361995
UNII
9J765S329G

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
ORAL
source: ndc

Resolved Composition

Strengths
  • 200 ug/1
source: ndc
Packaging
  • 90 TABLET in 1 BOTTLE (68071-3619-9)
source: ndc

Packages (1)

68071-3619-9 90 TABLET in 1 BOTTLE (68071-3619-9)

Ingredients (1)

levothyroxine sodium (200 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": "1ac85666-6200-3887-e063-6394a90a105e", "openfda": {"upc": ["0368071361995"], "unii": ["9J765S329G"], "rxcui": ["892251"], "spl_set_id": ["1ac856d1-7067-a71d-e063-6294a90acc7c"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (68071-3619-9)", "package_ndc": "68071-3619-9", "marketing_start_date": "20240613"}], "brand_name": "Levothyroxine sodium", "product_id": "68071-3619_1ac85666-6200-3887-e063-6394a90a105e", "dosage_form": "TABLET", "pharm_class": ["Thyroxine [CS]", "l-Thyroxine [EPC]"], "product_ndc": "68071-3619", "generic_name": "Levothyroxine Sodium", "labeler_name": "NuCare Pharmaceuticals,Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Levothyroxine sodium", "active_ingredients": [{"name": "LEVOTHYROXINE SODIUM", "strength": "200 ug/1"}], "application_number": "ANDA212399", "marketing_category": "ANDA", "marketing_start_date": "20201203", "listing_expiration_date": "20261231"}