Package 82868-001-30

Brand: levothyroxine sodium

Generic: levothyroxine sodium
NDC Package

Package Facts

Identity

Package NDC 82868-001-30
Digits Only 8286800130
Product NDC 82868-001
Description

30 TABLET in 1 BOTTLE (82868-001-30)

Marketing

Marketing Status
Marketed Since 2023-07-05
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": "483325a2-752b-f9c2-e063-6394a90ada32", "openfda": {"unii": ["9J765S329G"], "rxcui": ["892251"], "spl_set_id": ["ffc34bc6-5de5-addb-e053-6294a90a25be"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (82868-001-30)", "package_ndc": "82868-001-30", "marketing_start_date": "20230705"}], "brand_name": "Levothyroxine Sodium", "product_id": "82868-001_483325a2-752b-f9c2-e063-6394a90ada32", "dosage_form": "TABLET", "pharm_class": ["Thyroxine [CS]", "l-Thyroxine [EPC]"], "product_ndc": "82868-001", "generic_name": "Levothyroxine Sodium", "labeler_name": "Northwind Health Company, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Levothyroxine Sodium", "active_ingredients": [{"name": "LEVOTHYROXINE SODIUM", "strength": ".2 mg/1"}], "application_number": "ANDA209713", "marketing_category": "ANDA", "marketing_start_date": "20230705", "listing_expiration_date": "20271231"}