levothyroxine sodium

Generic: levothyroxine sodium

Labeler: major pharmaceuticals
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name levothyroxine sodium
Generic Name levothyroxine sodium
Labeler major pharmaceuticals
Dosage Form TABLET
Routes
ORAL
Active Ingredients

levothyroxine sodium .112 mg/1

Manufacturer
Major Pharmaceuticals

Identifiers & Regulatory

Product NDC 0904-6954
Product ID 0904-6954_942c00a3-b31c-48d5-a63d-6d394645ee1f
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 09046954
Hyphenated Format 0904-6954

Supplemental Identifiers

RxCUI
892246 966220 966221 966222 966224 966225 966248 966249 966253
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
  • .112 mg/1
source: ndc
Packaging
  • 100 BLISTER PACK in 1 CARTON (0904-6954-61) / 1 TABLET in 1 BLISTER PACK
source: ndc

Packages (1)

0904-6954-61 100 BLISTER PACK in 1 CARTON (0904-6954-61) / 1 TABLET in 1 BLISTER PACK

Ingredients (1)

levothyroxine sodium (.112 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": "942c00a3-b31c-48d5-a63d-6d394645ee1f", "openfda": {"unii": ["9J765S329G"], "rxcui": ["892246", "966220", "966221", "966222", "966224", "966225", "966248", "966249", "966253"], "spl_set_id": ["333642fd-93ae-4dc0-9c83-6d6b163c1c74"], "manufacturer_name": ["Major Pharmaceuticals"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 CARTON (0904-6954-61)  / 1 TABLET in 1 BLISTER PACK", "package_ndc": "0904-6954-61", "marketing_start_date": "20190320"}], "brand_name": "Levothyroxine Sodium", "product_id": "0904-6954_942c00a3-b31c-48d5-a63d-6d394645ee1f", "dosage_form": "TABLET", "pharm_class": ["Thyroxine [CS]", "l-Thyroxine [EPC]"], "product_ndc": "0904-6954", "generic_name": "Levothyroxine Sodium", "labeler_name": "Major Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Levothyroxine Sodium", "active_ingredients": [{"name": "LEVOTHYROXINE SODIUM", "strength": ".112 mg/1"}], "application_number": "ANDA209713", "marketing_category": "ANDA", "marketing_start_date": "20190320", "listing_expiration_date": "20261231"}