Package 70710-1835-1

Brand: levothyroxine sodium

Generic: levothyroxine sodium
NDC Package

Package Facts

Identity

Package NDC 70710-1835-1
Digits Only 7071018351
Product NDC 70710-1835
Product ID 70710-1835_2ef84f1a-cf9a-4e93-8b2b-08bf75befd9e
Description

1 VIAL, SINGLE-DOSE in 1 CARTON (70710-1835-1) / 5 mL in 1 VIAL, SINGLE-DOSE

Marketing

Marketing Status
Marketed Since 2024-11-01
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": ["INTRAVENOUS"], "spl_id": "2ef84f1a-cf9a-4e93-8b2b-08bf75befd9e", "openfda": {"unii": ["054I36CPMN"], "rxcui": ["966219", "1115267", "1115269"], "spl_set_id": ["bf8a952c-f05b-4814-b55a-ed04be015269"], "manufacturer_name": ["Zydus Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, SINGLE-DOSE in 1 CARTON (70710-1835-1)  / 5 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "70710-1835-1", "marketing_start_date": "20241101"}], "brand_name": "LEVOTHYROXINE SODIUM", "product_id": "70710-1835_2ef84f1a-cf9a-4e93-8b2b-08bf75befd9e", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Thyroxine [CS]", "l-Thyroxine [EPC]"], "product_ndc": "70710-1835", "generic_name": "levothyroxine sodium", "labeler_name": "Zydus Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "LEVOTHYROXINE SODIUM", "active_ingredients": [{"name": "LEVOTHYROXINE SODIUM ANHYDROUS", "strength": "500 ug/5mL"}], "application_number": "ANDA217066", "marketing_category": "ANDA", "marketing_start_date": "20241101", "listing_expiration_date": "20261231"}