levothyroxine sodium

Generic: levothyroxine sodium

Labeler: direct rx
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name levothyroxine sodium
Generic Name levothyroxine sodium
Labeler direct rx
Dosage Form TABLET
Routes
ORAL
Active Ingredients

levothyroxine sodium 75 ug/1

Manufacturer
DIRECT RX

Identifiers & Regulatory

Product NDC 72189-073
Product ID 72189-073_1922dbd9-96de-8652-e063-6294a90a0afe
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA021116
Listing Expiration 2026-12-31
Marketing Start 2020-07-30

Pharmacologic Class

Classes
thyroxine [cs] l-thyroxine [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72189073
Hyphenated Format 72189-073

Supplemental Identifiers

RxCUI
892246 966220 966221 966222 966224 966225 966248 966253 966270
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 NDA021116 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 75 ug/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (72189-073-30)
  • 90 TABLET in 1 BOTTLE (72189-073-90)
source: ndc

Packages (2)

72189-073-30 30 TABLET in 1 BOTTLE (72189-073-30) 72189-073-90 90 TABLET in 1 BOTTLE (72189-073-90)

Ingredients (1)

levothyroxine sodium (75 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": "1922dbd9-96de-8652-e063-6294a90a0afe", "openfda": {"unii": ["9J765S329G"], "rxcui": ["892246", "966220", "966221", "966222", "966224", "966225", "966248", "966253", "966270"], "spl_set_id": ["a5f15022-1166-09fe-e053-2a95a90aa218"], "manufacturer_name": ["DIRECT RX"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (72189-073-30)", "package_ndc": "72189-073-30", "marketing_start_date": "20200730"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (72189-073-90)", "package_ndc": "72189-073-90", "marketing_start_date": "20200730"}], "brand_name": "LEVOTHYROXINE SODIUM", "product_id": "72189-073_1922dbd9-96de-8652-e063-6294a90a0afe", "dosage_form": "TABLET", "pharm_class": ["Thyroxine [CS]", "l-Thyroxine [EPC]"], "product_ndc": "72189-073", "generic_name": "LEVOTHYROXINE SODIUM", "labeler_name": "DIRECT RX", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "LEVOTHYROXINE SODIUM", "active_ingredients": [{"name": "LEVOTHYROXINE SODIUM", "strength": "75 ug/1"}], "application_number": "NDA021116", "marketing_category": "NDA", "marketing_start_date": "20200730", "listing_expiration_date": "20261231"}