Package 70511-113-10

Brand: levothyroxine sodium

Generic: levothyroxine sodium anhydrous
NDC Package

Package Facts

Identity

Package NDC 70511-113-10
Digits Only 7051111310
Product NDC 70511-113
Product ID 70511-113_9efa2867-7721-478a-a1c3-e34eeb3a1937
Description

1 VIAL, SINGLE-USE in 1 CARTON (70511-113-10) / 5 mL in 1 VIAL, SINGLE-USE

Marketing

Marketing Status
Marketed Since 2018-12-27
Brand levothyroxine sodium
Generic levothyroxine sodium anhydrous
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": "9efa2867-7721-478a-a1c3-e34eeb3a1937", "openfda": {"unii": ["054I36CPMN"], "rxcui": ["966219", "1115267", "1115269"], "spl_set_id": ["4e9adc35-3aba-4a0d-9c4e-7e7ee2ffdabd"], "manufacturer_name": ["MAIA Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, SINGLE-USE in 1 CARTON (70511-113-10)  / 5 mL in 1 VIAL, SINGLE-USE", "package_ndc": "70511-113-10", "marketing_start_date": "20181227"}], "brand_name": "Levothyroxine Sodium", "product_id": "70511-113_9efa2867-7721-478a-a1c3-e34eeb3a1937", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Thyroxine [CS]", "l-Thyroxine [EPC]"], "product_ndc": "70511-113", "generic_name": "LEVOTHYROXINE SODIUM ANHYDROUS", "labeler_name": "MAIA Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Levothyroxine Sodium", "active_ingredients": [{"name": "LEVOTHYROXINE SODIUM ANHYDROUS", "strength": "500 ug/5mL"}], "application_number": "ANDA208749", "marketing_category": "ANDA", "marketing_start_date": "20181227", "listing_expiration_date": "20261231"}