Package 50090-7871-0

Brand: levothyroxine sodium

Generic: levothyroxine sodium
NDC Package

Package Facts

Identity

Package NDC 50090-7871-0
Digits Only 5009078710
Product NDC 50090-7871
Description

90 TABLET in 1 BOTTLE (50090-7871-0)

Marketing

Marketing Status
Marketed Since 2026-01-29
Brand levothyroxine sodium
Generic levothyroxine sodium
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "79026dbf-6797-431e-bae7-a8ee1477e5e5", "openfda": {"unii": ["9J765S329G"], "rxcui": ["966253"], "spl_set_id": ["62de26a8-d6fc-463f-abe6-4656228c3142"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (50090-7871-0)", "package_ndc": "50090-7871-0", "marketing_start_date": "20260129"}], "brand_name": "Levothyroxine sodium", "product_id": "50090-7871_79026dbf-6797-431e-bae7-a8ee1477e5e5", "dosage_form": "TABLET", "pharm_class": ["Thyroxine [CS]", "l-Thyroxine [EPC]"], "product_ndc": "50090-7871", "generic_name": "Levothyroxine Sodium", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Levothyroxine sodium", "active_ingredients": [{"name": "LEVOTHYROXINE SODIUM", "strength": "88 ug/1"}], "application_number": "ANDA212399", "marketing_category": "ANDA", "marketing_start_date": "20201125", "listing_expiration_date": "20271231"}