Package 63323-013-09

Brand: thiamine

Generic: thiamine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 63323-013-09
Digits Only 6332301309
Product NDC 63323-013
Product ID 63323-013_3b09217b-e746-4523-95fa-b78fad431e32
Description

25 VIAL, MULTI-DOSE in 1 TRAY (63323-013-09) / 2 mL in 1 VIAL, MULTI-DOSE (63323-013-21)

Marketing

Marketing Status
Marketed Since 2000-09-01
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": "3b09217b-e746-4523-95fa-b78fad431e32", "openfda": {"upc": ["0363323013219"], "unii": ["M572600E5P"], "rxcui": ["313324"], "spl_set_id": ["c3c9db74-95d4-487c-90c3-c810786fbaec"], "manufacturer_name": ["Fresenius Kabi USA, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL, MULTI-DOSE in 1 TRAY (63323-013-09)  / 2 mL in 1 VIAL, MULTI-DOSE (63323-013-21)", "package_ndc": "63323-013-09", "marketing_start_date": "20000901"}], "brand_name": "Thiamine", "product_id": "63323-013_3b09217b-e746-4523-95fa-b78fad431e32", "dosage_form": "INJECTION, SOLUTION", "product_ndc": "63323-013", "generic_name": "THIAMINE HYDROCHLORIDE", "labeler_name": "Fresenius Kabi USA, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Thiamine", "active_ingredients": [{"name": "THIAMINE HYDROCHLORIDE", "strength": "100 mg/mL"}], "application_number": "ANDA080556", "marketing_category": "ANDA", "marketing_start_date": "20000901", "listing_expiration_date": "20271231"}