Package 83270-006-01

Brand: levothyroxine sodium

Generic: levothyroxine sodium anhydrous
NDC Package

Package Facts

Identity

Package NDC 83270-006-01
Digits Only 8327000601
Product NDC 83270-006
Description

1 VIAL, SINGLE-DOSE in 1 CARTON (83270-006-01) / 5 mL in 1 VIAL, SINGLE-DOSE

Marketing

Marketing Status
Marketed Since 2025-09-30
Brand levothyroxine sodium
Generic levothyroxine sodium anhydrous
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "35b79b8a-71ee-374b-e063-6394a90a887a", "openfda": {"upc": ["0383270006010", "0383270007017", "0383270008014"], "unii": ["054I36CPMN"], "rxcui": ["966219", "1115267", "1115269"], "spl_set_id": ["ae9954a5-e196-449c-abea-ebe4afbee517"], "manufacturer_name": ["ONESOURCE SPECIALTY PHARMA LIMITED"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, SINGLE-DOSE in 1 CARTON (83270-006-01)  / 5 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "83270-006-01", "marketing_start_date": "20250930"}], "brand_name": "Levothyroxine Sodium", "product_id": "83270-006_35b79b8a-71ee-374b-e063-6394a90a887a", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Thyroxine [CS]", "l-Thyroxine [EPC]"], "product_ndc": "83270-006", "generic_name": "LEVOTHYROXINE SODIUM ANHYDROUS", "labeler_name": "ONESOURCE SPECIALTY PHARMA LIMITED", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Levothyroxine Sodium", "active_ingredients": [{"name": "LEVOTHYROXINE SODIUM ANHYDROUS", "strength": "100 ug/5mL"}], "application_number": "ANDA216729", "marketing_category": "ANDA", "marketing_start_date": "20250815", "listing_expiration_date": "20261231"}