Package 50090-6602-0

Brand: levothyroxine sodium

Generic: levothyroxine sodium
NDC Package

Package Facts

Identity

Package NDC 50090-6602-0
Digits Only 5009066020
Product NDC 50090-6602
Product ID 50090-6602_d79c0046-2c71-47a4-9b06-3ffe57e4243e
Description

90 TABLET in 1 BOTTLE (50090-6602-0)

Marketing

Marketing Status
Marketed Since 2023-08-22
Brand levothyroxine sodium
Generic levothyroxine sodium
Sample Package No

Linked Drug Pages (0)

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Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "d79c0046-2c71-47a4-9b06-3ffe57e4243e", "openfda": {"unii": ["9J765S329G"], "rxcui": ["966248"], "spl_set_id": ["d5b11dac-1acd-4aa2-b837-e3b90d4f6922"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (50090-6602-0)", "package_ndc": "50090-6602-0", "marketing_start_date": "20230822"}], "brand_name": "Levothyroxine sodium", "product_id": "50090-6602_d79c0046-2c71-47a4-9b06-3ffe57e4243e", "dosage_form": "TABLET", "pharm_class": ["Thyroxine [CS]", "l-Thyroxine [EPC]"], "product_ndc": "50090-6602", "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": "112 ug/1"}], "application_number": "ANDA212399", "marketing_category": "ANDA", "marketing_start_date": "20201125", "listing_expiration_date": "20271231"}