Package 68071-3787-9

Brand: levothyroxine sodium

Generic: levothyroxine sodium
NDC Package

Package Facts

Identity

Package NDC 68071-3787-9
Digits Only 6807137879
Product NDC 68071-3787
Product ID 68071-3787_2cf49703-3f83-f503-e063-6394a90a61f6
Description

90 TABLET in 1 BOTTLE (68071-3787-9)

Marketing

Marketing Status
Marketed Since 2025-01-30
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": "2cf49703-3f83-f503-e063-6394a90a61f6", "openfda": {"upc": ["0368071378795"], "unii": ["9J765S329G"], "rxcui": ["892251"], "spl_set_id": ["2cf48978-d996-f5ba-e063-6294a90a8824"], "manufacturer_name": ["NuCare Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (68071-3787-9)", "package_ndc": "68071-3787-9", "marketing_start_date": "20250130"}], "brand_name": "Levothyroxine Sodium", "product_id": "68071-3787_2cf49703-3f83-f503-e063-6394a90a61f6", "dosage_form": "TABLET", "pharm_class": ["Thyroxine [CS]", "l-Thyroxine [EPC]"], "product_ndc": "68071-3787", "generic_name": "Levothyroxine Sodium", "labeler_name": "NuCare Pharmaceuticals, Inc.", "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": "20190320", "listing_expiration_date": "20261231"}