Package 50090-7071-0

Brand: levothyroxine sodium

Generic: levothyroxine sodium
NDC Package

Package Facts

Identity

Package NDC 50090-7071-0
Digits Only 5009070710
Product NDC 50090-7071
Product ID 50090-7071_522656de-372c-4f99-9cd3-33343e68215e
Description

90 TABLET in 1 BOTTLE (50090-7071-0)

Marketing

Marketing Status
Marketed Since 2024-01-19
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": "522656de-372c-4f99-9cd3-33343e68215e", "openfda": {"unii": ["9J765S329G"], "rxcui": ["966220"], "spl_set_id": ["f5fc0f34-744c-4e03-ae9f-e017e4033139"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (50090-7071-0)", "package_ndc": "50090-7071-0", "marketing_start_date": "20240119"}], "brand_name": "Levothyroxine Sodium", "product_id": "50090-7071_522656de-372c-4f99-9cd3-33343e68215e", "dosage_form": "TABLET", "pharm_class": ["Thyroxine [CS]", "l-Thyroxine [EPC]"], "product_ndc": "50090-7071", "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": ".025 mg/1"}], "application_number": "ANDA209713", "marketing_category": "ANDA", "marketing_start_date": "20190320", "listing_expiration_date": "20261231"}