Package 70518-3208-0

Brand: levothyroxine sodium

Generic: levothyroxine sodium
NDC Package

Package Facts

Identity

Package NDC 70518-3208-0
Digits Only 7051832080
Product NDC 70518-3208
Product ID 70518-3208_44e5cc14-cb46-6ab2-e063-6394a90a291e
Description

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

Marketing

Marketing Status
Marketed Since 2022-08-07
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": "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"}