thiamine hydrochloride

Generic: thiamine hydrochloride

Labeler: sagent pharmaceuticals
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name thiamine hydrochloride
Generic Name thiamine hydrochloride
Labeler sagent pharmaceuticals
Dosage Form INJECTION, SOLUTION
Routes
INTRAMUSCULAR INTRAVENOUS
Active Ingredients

thiamine hydrochloride 100 mg/mL

Manufacturer
Sagent Pharmaceuticals

Identifiers & Regulatory

Product NDC 25021-500
Product ID 25021-500_644d12b5-9a05-47dc-9e1c-d8f6fe9bbec2
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA206106
Listing Expiration 2026-12-31
Marketing Start 2021-01-20

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 25021500
Hyphenated Format 25021-500

Supplemental Identifiers

RxCUI
313324
UNII
M572600E5P

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name thiamine hydrochloride (source: ndc)
Generic Name thiamine hydrochloride (source: ndc)
Application Number ANDA206106 (source: ndc)
Routes
INTRAMUSCULAR INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 100 mg/mL
source: ndc
Packaging
  • 25 VIAL in 1 CARTON (25021-500-02) / 2 mL in 1 VIAL
source: ndc

Packages (1)

Ingredients (1)

thiamine hydrochloride (100 mg/mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "644d12b5-9a05-47dc-9e1c-d8f6fe9bbec2", "openfda": {"unii": ["M572600E5P"], "rxcui": ["313324"], "spl_set_id": ["5982cf83-01d6-4acb-8373-339079b8a76e"], "manufacturer_name": ["Sagent Pharmaceuticals"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL in 1 CARTON (25021-500-02)  / 2 mL in 1 VIAL", "package_ndc": "25021-500-02", "marketing_start_date": "20210120"}], "brand_name": "thiamine hydrochloride", "product_id": "25021-500_644d12b5-9a05-47dc-9e1c-d8f6fe9bbec2", "dosage_form": "INJECTION, SOLUTION", "product_ndc": "25021-500", "generic_name": "thiamine hydrochloride", "labeler_name": "Sagent Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "thiamine hydrochloride", "active_ingredients": [{"name": "THIAMINE HYDROCHLORIDE", "strength": "100 mg/mL"}], "application_number": "ANDA206106", "marketing_category": "ANDA", "marketing_start_date": "20210120", "listing_expiration_date": "20261231"}