levothyroxine sodium

Generic: levothyroxine sodium

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

Drug Facts

Product Profile

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

levothyroxine sodium .125 mg/1

Manufacturer
NuCarePharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 68071-3692
Product ID 68071-3692_23808d9e-74ef-0104-e063-6394a90a1fae
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA209713
Listing Expiration 2026-12-31
Marketing Start 2019-03-20

Pharmacologic Class

Classes
thyroxine [cs] l-thyroxine [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 680713692
Hyphenated Format 68071-3692

Supplemental Identifiers

RxCUI
966224
UPC
0368071369298
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 ANDA209713 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • .125 mg/1
source: ndc
Packaging
  • 90 TABLET in 1 BOTTLE (68071-3692-9)
source: ndc

Packages (1)

68071-3692-9 90 TABLET in 1 BOTTLE (68071-3692-9)

Ingredients (1)

levothyroxine sodium (.125 mg/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": "23808d9e-74ef-0104-e063-6394a90a1fae", "openfda": {"upc": ["0368071369298"], "unii": ["9J765S329G"], "rxcui": ["966224"], "spl_set_id": ["2380859a-5b65-f88f-e063-6394a90aa4e2"], "manufacturer_name": ["NuCarePharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (68071-3692-9)", "package_ndc": "68071-3692-9", "marketing_start_date": "20241002"}], "brand_name": "Levothyroxine Sodium", "product_id": "68071-3692_23808d9e-74ef-0104-e063-6394a90a1fae", "dosage_form": "TABLET", "pharm_class": ["Thyroxine [CS]", "l-Thyroxine [EPC]"], "product_ndc": "68071-3692", "generic_name": "Levothyroxine Sodium", "labeler_name": "NuCarePharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Levothyroxine Sodium", "active_ingredients": [{"name": "LEVOTHYROXINE SODIUM", "strength": ".125 mg/1"}], "application_number": "ANDA209713", "marketing_category": "ANDA", "marketing_start_date": "20190320", "listing_expiration_date": "20261231"}