Package 50090-6660-0

Brand: levothyroxine sodium

Generic: levothyroxine sodium
NDC Package

Package Facts

Identity

Package NDC 50090-6660-0
Digits Only 5009066600
Product NDC 50090-6660
Description

90 TABLET in 1 BOTTLE (50090-6660-0)

Marketing

Marketing Status
Marketed Since 2023-08-30
Brand levothyroxine sodium
Generic levothyroxine sodium
Sample Package No

Linked Drug Pages (0)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "bad46086-cfd6-43b1-8725-a2c391d9215e", "openfda": {"unii": ["9J765S329G"], "rxcui": ["966221"], "spl_set_id": ["eb149423-070f-49ae-ab18-5afee09d06fb"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (50090-6660-0)", "package_ndc": "50090-6660-0", "marketing_start_date": "20230830"}], "brand_name": "Levothyroxine sodium", "product_id": "50090-6660_bad46086-cfd6-43b1-8725-a2c391d9215e", "dosage_form": "TABLET", "pharm_class": ["Thyroxine [CS]", "l-Thyroxine [EPC]"], "product_ndc": "50090-6660", "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": "50 ug/1"}], "application_number": "ANDA212399", "marketing_category": "ANDA", "marketing_start_date": "20201125", "listing_expiration_date": "20261231"}