NDC directory

Thiamine Hydrochloride

Lifestar Pharma LLC · INJECTION, SOLUTION

70756-684ANDA
Product NDC
70756-684
Generic name
Thiamine Hydrochloride
Labeler name
Lifestar Pharma LLC
Brand name
Thiamine Hydrochloride
Finished
true
Listing expiration date
20271231
Marketing category
ANDA
Dosage form
INJECTION, SOLUTION
SPL ID
f060a329-8fde-44c1-8750-03b85e478d58
Product type
HUMAN PRESCRIPTION DRUG
Marketing start date
20261001
Product ID
70756-684_f060a329-8fde-44c1-8750-03b85e478d58
Application number
ANDA220513
Brand name base
Thiamine Hydrochloride
Active ingredients
  1. Name
    THIAMINE HYDROCHLORIDE
    Strength
    100 mg/mL
Packaging
  1. Package NDC
    70756-684-25
    Description
    25 VIAL, MULTI-DOSE in 1 CARTON (70756-684-25) / 2 mL in 1 VIAL, MULTI-DOSE (70756-684-82)
    Marketing start date
    20261001
    Sample
    false
Route
INTRAMUSCULAR, INTRAVENOUS
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Data from openFDA, FDA's public API. FDA says not to rely on it to make decisions about medical care and to treat every result as unvalidated; confirm against FDA's own record and the product labeling. Not medical or legal advice.