thiamine hydrochloride

Generic: thiamine hydrochloride

Labeler: remedyrepack inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name thiamine hydrochloride
Generic Name thiamine hydrochloride
Labeler remedyrepack inc.
Dosage Form INJECTION, SOLUTION
Routes
INTRAMUSCULAR INTRAVENOUS
Active Ingredients

thiamine hydrochloride 100 mg/mL

Manufacturer
REMEDYREPACK INC.

Identifiers & Regulatory

Product NDC 70518-4230
Product ID 70518-4230_4005d19e-7cd8-f2db-e063-6394a90a9e7e
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA080575
Listing Expiration 2026-12-31
Marketing Start 2024-11-13

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 705184230
Hyphenated Format 70518-4230

Supplemental Identifiers

RxCUI
313324
UNII
M572600E5P

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 ANDA080575 (source: ndc)
Routes
INTRAMUSCULAR INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 100 mg/mL
source: ndc
Packaging
  • 25 VIAL in 1 CARTON (70518-4230-0) / 2 mL in 1 VIAL (70518-4230-1)
source: ndc

Packages (1)

70518-4230-0 25 VIAL in 1 CARTON (70518-4230-0) / 2 mL in 1 VIAL (70518-4230-1)

Ingredients (1)

thiamine hydrochloride (100 mg/mL)

Linked Drug Pages (1)

Thiamine Hydrochloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "4005d19e-7cd8-f2db-e063-6394a90a9e7e", "openfda": {"unii": ["M572600E5P"], "rxcui": ["313324"], "spl_set_id": ["0f38c4ba-cebf-49f4-b0a6-8a5d3ebf618c"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL in 1 CARTON (70518-4230-0)  / 2 mL in 1 VIAL (70518-4230-1)", "package_ndc": "70518-4230-0", "marketing_start_date": "20241113"}], "brand_name": "Thiamine Hydrochloride", "product_id": "70518-4230_4005d19e-7cd8-f2db-e063-6394a90a9e7e", "dosage_form": "INJECTION, SOLUTION", "product_ndc": "70518-4230", "generic_name": "Thiamine Hydrochloride", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Thiamine Hydrochloride", "active_ingredients": [{"name": "THIAMINE HYDROCHLORIDE", "strength": "100 mg/mL"}], "application_number": "ANDA080575", "marketing_category": "ANDA", "marketing_start_date": "20241113", "listing_expiration_date": "20261231"}