Package 72603-139-25

Brand: thiamine

Generic: thiamine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72603-139-25
Digits Only 7260313925
Product NDC 72603-139
Product ID 72603-139_f4790075-a740-4550-9d4c-69a00dac354c
Description

25 VIAL, MULTI-DOSE in 1 CARTON (72603-139-25) / 2 mL in 1 VIAL, MULTI-DOSE (72603-139-01)

Marketing

Marketing Status
Marketed Since 2023-04-20
Brand thiamine
Generic thiamine hydrochloride
Sample Package No

Linked Drug Pages (1)

Thiamine ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "f4790075-a740-4550-9d4c-69a00dac354c", "openfda": {"upc": ["0372603139013", "0372603139259"], "unii": ["M572600E5P"], "rxcui": ["313324"], "spl_set_id": ["f4790075-a740-4550-9d4c-69a00dac354c"], "manufacturer_name": ["NorthStar Rx LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL, MULTI-DOSE in 1 CARTON (72603-139-25)  / 2 mL in 1 VIAL, MULTI-DOSE (72603-139-01)", "package_ndc": "72603-139-25", "marketing_start_date": "20230420"}], "brand_name": "Thiamine", "product_id": "72603-139_f4790075-a740-4550-9d4c-69a00dac354c", "dosage_form": "INJECTION, SOLUTION", "product_ndc": "72603-139", "generic_name": "Thiamine Hydrochloride", "labeler_name": "NorthStar Rx LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Thiamine", "active_ingredients": [{"name": "THIAMINE HYDROCHLORIDE", "strength": "100 mg/mL"}], "application_number": "ANDA215692", "marketing_category": "ANDA", "marketing_start_date": "20230420", "listing_expiration_date": "20261231"}