Package 72789-272-90

Brand: levothyroxine sodium

Generic: levothyroxine sodium
NDC Package

Package Facts

Identity

Package NDC 72789-272-90
Digits Only 7278927290
Product NDC 72789-272
Description

90 TABLET in 1 BOTTLE, PLASTIC (72789-272-90)

Marketing

Marketing Status
Marketed Since 2022-09-23
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": "4bad91ed-0e19-2d1e-e063-6394a90a669f", "openfda": {"upc": ["0372789272900"], "unii": ["9J765S329G"], "rxcui": ["966221"], "spl_set_id": ["70a9bb5c-2259-405e-8d89-cc1db8c70743"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (72789-272-30)", "package_ndc": "72789-272-30", "marketing_start_date": "20220916"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (72789-272-90)", "package_ndc": "72789-272-90", "marketing_start_date": "20220923"}], "brand_name": "Levothyroxine sodium", "product_id": "72789-272_4bad91ed-0e19-2d1e-e063-6394a90a669f", "dosage_form": "TABLET", "pharm_class": ["Thyroxine [CS]", "l-Thyroxine [EPC]"], "product_ndc": "72789-272", "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": "50 ug/1"}], "application_number": "ANDA212399", "marketing_category": "ANDA", "marketing_start_date": "20201125", "listing_expiration_date": "20271231"}