Package 31722-363-32

Brand: thiamine hydrochloride

Generic: thiamine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 31722-363-32
Digits Only 3172236332
Product NDC 31722-363
Description

25 VIAL, MULTI-DOSE in 1 TRAY (31722-363-32) / 2 mL in 1 VIAL, MULTI-DOSE (31722-363-31)

Marketing

Marketing Status
Marketed Since 2024-11-06
Brand thiamine hydrochloride
Generic thiamine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "2d388a74-ef70-f1a1-e063-6294a90a9878", "openfda": {"upc": ["0331722363310"], "unii": ["M572600E5P"], "rxcui": ["313324"], "spl_set_id": ["2d402a31-3240-42a0-bd34-8fccd6a792d3"], "manufacturer_name": ["Camber Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL, MULTI-DOSE in 1 TRAY (31722-363-32)  / 2 mL in 1 VIAL, MULTI-DOSE (31722-363-31)", "package_ndc": "31722-363-32", "marketing_start_date": "20241106"}], "brand_name": "Thiamine Hydrochloride", "product_id": "31722-363_2d388a74-ef70-f1a1-e063-6294a90a9878", "dosage_form": "INJECTION, SOLUTION", "product_ndc": "31722-363", "generic_name": "Thiamine Hydrochloride", "labeler_name": "Camber Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Thiamine Hydrochloride", "active_ingredients": [{"name": "THIAMINE HYDROCHLORIDE", "strength": "100 mg/mL"}], "application_number": "ANDA218471", "marketing_category": "ANDA", "marketing_start_date": "20241106", "listing_expiration_date": "20261231"}