Package 63323-885-14

Brand: levothyroxine sodium

Generic: levothyroxine sodium
NDC Package

Package Facts

Identity

Package NDC 63323-885-14
Digits Only 6332388514
Product NDC 63323-885
Product ID 63323-885_6514086f-834b-4c0c-82a1-c95338ef42a0
Description

1 VIAL, SINGLE-DOSE in 1 CARTON (63323-885-14) / 5 mL in 1 VIAL, SINGLE-DOSE

Marketing

Marketing Status
Marketed Since 2018-05-29
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": "6514086f-834b-4c0c-82a1-c95338ef42a0", "openfda": {"upc": ["0363323885144"], "unii": ["9J765S329G"], "rxcui": ["2166193"], "spl_set_id": ["388a1f15-8c1c-46a5-997f-7f326f696b59"], "manufacturer_name": ["Fresenius Kabi USA, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, SINGLE-DOSE in 1 CARTON (63323-885-14)  / 5 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "63323-885-14", "marketing_start_date": "20180529"}], "brand_name": "Levothyroxine Sodium", "product_id": "63323-885_6514086f-834b-4c0c-82a1-c95338ef42a0", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Thyroxine [CS]", "l-Thyroxine [EPC]"], "product_ndc": "63323-885", "generic_name": "Levothyroxine Sodium", "labeler_name": "Fresenius Kabi USA, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Levothyroxine Sodium", "active_ingredients": [{"name": "LEVOTHYROXINE SODIUM", "strength": "20 ug/mL"}], "application_number": "NDA210632", "marketing_category": "NDA", "marketing_start_date": "20180529", "listing_expiration_date": "20261231"}