Package 72789-297-30

Brand: levothyroxine sodium

Generic: levothyroxine sodium
NDC Package

Package Facts

Identity

Package NDC 72789-297-30
Digits Only 7278929730
Product NDC 72789-297
Product ID 72789-297_4bae1773-79fb-e98a-e063-6394a90a3266
Description

30 TABLET in 1 BOTTLE, PLASTIC (72789-297-30)

Marketing

Marketing Status
Marketed Since 2023-01-11
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": "4bae1773-79fb-e98a-e063-6394a90a3266", "openfda": {"upc": ["0372789297309"], "unii": ["9J765S329G"], "rxcui": ["892246"], "spl_set_id": ["6f4998ac-0714-4f5d-8944-9e6902b9f0a6"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (72789-297-30)", "package_ndc": "72789-297-30", "marketing_start_date": "20230111"}], "brand_name": "Levothyroxine sodium", "product_id": "72789-297_4bae1773-79fb-e98a-e063-6394a90a3266", "dosage_form": "TABLET", "pharm_class": ["Thyroxine [CS]", "l-Thyroxine [EPC]"], "product_ndc": "72789-297", "generic_name": "Levothyroxine Sodium", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Levothyroxine sodium", "active_ingredients": [{"name": "LEVOTHYROXINE SODIUM", "strength": "100 ug/1"}], "application_number": "ANDA212399", "marketing_category": "ANDA", "marketing_start_date": "20201210", "listing_expiration_date": "20271231"}