Package 82804-246-30

Brand: levothyroxine sodium

Generic: levothyroxine sodium
NDC Package

Package Facts

Identity

Package NDC 82804-246-30
Digits Only 8280424630
Product NDC 82804-246
Product ID 82804-246_bcf10012-8920-4737-92f5-7401ee0c5894
Description

30 TABLET in 1 BOTTLE (82804-246-30)

Marketing

Marketing Status
Marketed Since 2025-10-02
Brand levothyroxine sodium
Generic levothyroxine sodium
Sample Package No

Linked Drug Pages (1)

Levothyroxine Sodium ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "bcf10012-8920-4737-92f5-7401ee0c5894", "openfda": {"upc": ["0382804246304"], "unii": ["9J765S329G"], "rxcui": ["966224"], "spl_set_id": ["bcf10012-8920-4737-92f5-7401ee0c5894"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (82804-246-30)", "package_ndc": "82804-246-30", "marketing_start_date": "20251002"}], "brand_name": "Levothyroxine Sodium", "product_id": "82804-246_bcf10012-8920-4737-92f5-7401ee0c5894", "dosage_form": "TABLET", "pharm_class": ["Thyroxine [CS]", "l-Thyroxine [EPC]"], "product_ndc": "82804-246", "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": ".125 mg/1"}], "application_number": "ANDA209713", "marketing_category": "ANDA", "marketing_start_date": "20190320", "listing_expiration_date": "20261231"}