Package 82804-168-30

Brand: levothyroxine sodium

Generic: levothyroxine sodium
NDC Package

Package Facts

Identity

Package NDC 82804-168-30
Digits Only 8280416830
Product NDC 82804-168
Description

30 TABLET in 1 BOTTLE (82804-168-30)

Marketing

Marketing Status
Marketed Since 2024-12-09
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": "678b11e4-a8a5-4b9a-a937-517c9320372f", "openfda": {"upc": ["0382804168309"], "unii": ["9J765S329G"], "rxcui": ["966220"], "spl_set_id": ["576dcd01-d151-42ac-acd1-480a13bae176"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (82804-168-30)", "package_ndc": "82804-168-30", "marketing_start_date": "20241209"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (82804-168-90)", "package_ndc": "82804-168-90", "marketing_start_date": "20241223"}], "brand_name": "Levothyroxine sodium", "product_id": "82804-168_678b11e4-a8a5-4b9a-a937-517c9320372f", "dosage_form": "TABLET", "pharm_class": ["Thyroxine [CS]", "l-Thyroxine [EPC]"], "product_ndc": "82804-168", "generic_name": "Levothyroxine Sodium", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Levothyroxine sodium", "active_ingredients": [{"name": "LEVOTHYROXINE SODIUM", "strength": "25 ug/1"}], "application_number": "ANDA212399", "marketing_category": "ANDA", "marketing_start_date": "20201210", "listing_expiration_date": "20261231"}