thiamine hydrochloride injection, solution
Generic: thiamine hydrochloride injection, solution
Labeler: hf acquisition co llc, dba healthfirstDrug Facts
Product Profile
Brand Name
thiamine hydrochloride injection, solution
Generic Name
thiamine hydrochloride injection, solution
Labeler
hf acquisition co llc, dba healthfirst
Dosage Form
INJECTION, SOLUTION
Routes
Active Ingredients
thiamine hydrochloride 100 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
51662-1635
Product ID
51662-1635_3972cf2f-88ce-e507-e063-6394a90a8da5
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA080571
Listing Expiration
2026-12-31
Marketing Start
2023-09-26
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
516621635
Hyphenated Format
51662-1635
Supplemental Identifiers
RxCUI
UNII
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 injection, solution (source: ndc)
Generic Name
thiamine hydrochloride injection, solution (source: ndc)
Application Number
ANDA080571 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 100 mg/mL
Packaging
- 2 mL in 1 VIAL, MULTI-DOSE (51662-1635-1)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "3972cf2f-88ce-e507-e063-6394a90a8da5", "openfda": {"unii": ["M572600E5P"], "rxcui": ["313324"], "spl_set_id": ["06446e9a-0e85-0623-e063-6294a90ac403"], "manufacturer_name": ["HF Acquisition Co LLC, DBA HealthFirst"]}, "finished": true, "packaging": [{"sample": false, "description": "2 mL in 1 VIAL, MULTI-DOSE (51662-1635-1)", "package_ndc": "51662-1635-1", "marketing_start_date": "20230926"}], "brand_name": "THIAMINE HYDROCHLORIDE injection, solution", "product_id": "51662-1635_3972cf2f-88ce-e507-e063-6394a90a8da5", "dosage_form": "INJECTION, SOLUTION", "product_ndc": "51662-1635", "generic_name": "THIAMINE HYDROCHLORIDE injection, solution", "labeler_name": "HF Acquisition Co LLC, DBA HealthFirst", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "THIAMINE HYDROCHLORIDE injection, solution", "active_ingredients": [{"name": "THIAMINE HYDROCHLORIDE", "strength": "100 mg/mL"}], "application_number": "ANDA080571", "marketing_category": "ANDA", "marketing_start_date": "20230926", "listing_expiration_date": "20261231"}