levothyroxine sodium

Generic: levothyroxine sodium

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

Drug Facts

Product Profile

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

levothyroxine sodium 50 ug/1

Manufacturer
REMEDYREPACK INC.

Identifiers & Regulatory

Product NDC 70518-3208
Product ID 70518-3208_44e5cc14-cb46-6ab2-e063-6394a90a291e
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA212399
Listing Expiration 2026-12-31
Marketing Start 2022-08-07

Pharmacologic Class

Classes
thyroxine [cs] l-thyroxine [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 705183208
Hyphenated Format 70518-3208

Supplemental Identifiers

RxCUI
966221
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 ANDA212399 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 ug/1
source: ndc
Packaging
  • 90 TABLET in 1 BOTTLE (70518-3208-0)
source: ndc

Packages (1)

70518-3208-0 90 TABLET in 1 BOTTLE (70518-3208-0)

Ingredients (1)

levothyroxine sodium (50 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": "44e5cc14-cb46-6ab2-e063-6394a90a291e", "openfda": {"unii": ["9J765S329G"], "rxcui": ["966221"], "spl_set_id": ["c7d5b71b-e983-4b1a-bfc2-d2343cf8668c"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (70518-3208-0)", "package_ndc": "70518-3208-0", "marketing_start_date": "20220807"}], "brand_name": "Levothyroxine sodium", "product_id": "70518-3208_44e5cc14-cb46-6ab2-e063-6394a90a291e", "dosage_form": "TABLET", "pharm_class": ["Thyroxine [CS]", "l-Thyroxine [EPC]"], "product_ndc": "70518-3208", "generic_name": "Levothyroxine Sodium", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Levothyroxine sodium", "active_ingredients": [{"name": "LEVOTHYROXINE SODIUM", "strength": "50 ug/1"}], "application_number": "ANDA212399", "marketing_category": "ANDA", "marketing_start_date": "20220807", "listing_expiration_date": "20261231"}