levothyroxine sodium

Generic: levothyroxine sodium

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

Drug Facts

Product Profile

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

levothyroxine sodium .15 mg/1

Manufacturer
Lupin Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 68180-973
Product ID 68180-973_94052e3d-58b2-4f4b-8223-a47281c1a592
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 68180973
Hyphenated Format 68180-973

Supplemental Identifiers

RxCUI
892246 892251 892255 966220 966221 966222 966224 966225 966248 966249 966253 966270
UPC
0368180973010 0368180971016 0368180972013 0368180969013 0368180966012 0368180970019 0368180968016 0368180967019 0368180965015 0368180976011 0368180974017
UNII
9J765S329G

Packaging Origin

Original Packager
true

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
  • .15 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (68180-973-01)
  • 1000 TABLET in 1 BOTTLE (68180-973-03)
  • 90 TABLET in 1 BOTTLE (68180-973-09)
source: ndc

Packages (3)

68180-973-01 100 TABLET in 1 BOTTLE (68180-973-01) 68180-973-03 1000 TABLET in 1 BOTTLE (68180-973-03) 68180-973-09 90 TABLET in 1 BOTTLE (68180-973-09)

Ingredients (1)

levothyroxine sodium (.15 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": "94052e3d-58b2-4f4b-8223-a47281c1a592", "openfda": {"upc": ["0368180973010", "0368180971016", "0368180972013", "0368180969013", "0368180966012", "0368180970019", "0368180968016", "0368180967019", "0368180965015", "0368180976011", "0368180974017"], "unii": ["9J765S329G"], "rxcui": ["892246", "892251", "892255", "966220", "966221", "966222", "966224", "966225", "966248", "966249", "966253", "966270"], "spl_set_id": ["18717e58-89fb-4e2f-93b6-d6ac3e988d37"], "manufacturer_name": ["Lupin Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (68180-973-01)", "package_ndc": "68180-973-01", "marketing_start_date": "20190320"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (68180-973-03)", "package_ndc": "68180-973-03", "marketing_start_date": "20190320"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (68180-973-09)", "package_ndc": "68180-973-09", "marketing_start_date": "20190320"}], "brand_name": "Levothyroxine Sodium", "product_id": "68180-973_94052e3d-58b2-4f4b-8223-a47281c1a592", "dosage_form": "TABLET", "pharm_class": ["Thyroxine [CS]", "l-Thyroxine [EPC]"], "product_ndc": "68180-973", "generic_name": "Levothyroxine Sodium", "labeler_name": "Lupin Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Levothyroxine Sodium", "active_ingredients": [{"name": "LEVOTHYROXINE SODIUM", "strength": ".15 mg/1"}], "application_number": "ANDA209713", "marketing_category": "ANDA", "marketing_start_date": "20190320", "listing_expiration_date": "20261231"}