Package 63323-648-94

Brand: levothyroxine sodium

Generic: levothyroxine sodium anhydrous
NDC Package

Package Facts

Identity

Package NDC 63323-648-94
Digits Only 6332364894
Product NDC 63323-648
Product ID 63323-648_74ccf7df-fab4-4a59-b7b9-eb531ec49c37
Description

1 VIAL, SINGLE-DOSE in 1 CARTON (63323-648-94) / 5 mL in 1 VIAL, SINGLE-DOSE

Marketing

Marketing Status
Marketed Since 2011-06-24
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": "74ccf7df-fab4-4a59-b7b9-eb531ec49c37", "openfda": {"unii": ["054I36CPMN"], "rxcui": ["966219", "1115267"], "spl_set_id": ["152d071f-d4aa-46d2-b397-61c1cabdd86d"], "manufacturer_name": ["Fresenius Kabi USA, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, SINGLE-DOSE in 1 CARTON (63323-648-94)  / 5 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "63323-648-94", "marketing_start_date": "20110624"}], "brand_name": "Levothyroxine Sodium", "product_id": "63323-648_74ccf7df-fab4-4a59-b7b9-eb531ec49c37", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Thyroxine [CS]", "l-Thyroxine [EPC]"], "product_ndc": "63323-648", "generic_name": "LEVOTHYROXINE SODIUM ANHYDROUS", "labeler_name": "Fresenius Kabi USA, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Levothyroxine Sodium", "active_ingredients": [{"name": "LEVOTHYROXINE SODIUM ANHYDROUS", "strength": "500 ug/5mL"}], "application_number": "NDA202231", "marketing_category": "NDA", "marketing_start_date": "20110624", "listing_expiration_date": "20261231"}