levothyroxine sodium

Generic: levothyroxine sodium

Labeler: direct rx
NDC Directory HUMAN PRESCRIPTION DRUG ANDA 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 .075 mg/1

Manufacturer
DIRECT RX

Identifiers & Regulatory

Product NDC 72189-107
Product ID 72189-107_1922dbd9-96de-8652-e063-6294a90a0afe
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA209713
Listing Expiration 2026-12-31
Marketing Start 2020-05-18

Pharmacologic Class

Classes
thyroxine [cs] l-thyroxine [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72189107
Hyphenated Format 72189-107

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 ANDA209713 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • .075 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (72189-107-30)
  • 90 TABLET in 1 BOTTLE (72189-107-90)
source: ndc

Packages (2)

Ingredients (1)

levothyroxine sodium (.075 mg/1)

Linked Drug Pages (1)

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 (72189-107-30)", "package_ndc": "72189-107-30", "marketing_start_date": "20200518"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (72189-107-90)", "package_ndc": "72189-107-90", "marketing_start_date": "20200518"}], "brand_name": "LEVOTHYROXINE SODIUM", "product_id": "72189-107_1922dbd9-96de-8652-e063-6294a90a0afe", "dosage_form": "TABLET", "pharm_class": ["Thyroxine [CS]", "l-Thyroxine [EPC]"], "product_ndc": "72189-107", "generic_name": "LEVOTHYROXINE SODIUM", "labeler_name": "DIRECT RX", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "LEVOTHYROXINE SODIUM", "active_ingredients": [{"name": "LEVOTHYROXINE SODIUM", "strength": ".075 mg/1"}], "application_number": "ANDA209713", "marketing_category": "ANDA", "marketing_start_date": "20200518", "listing_expiration_date": "20261231"}