NDC product

Multiple Vitamins (Adult) Pharmacy Bulk Package

NDC 60505-6191 · Apotex Corp.

Key facts

Product NDC 60505-6191
Proprietary name Multiple Vitamins (Adult) Pharmacy Bulk Package
Nonproprietary name Ascorbic Acid, Vitamin A Palmitate, Cholecalciferol, Thiamine Hydrochloride, Riboflavin 5 phosphate sodium, Pyridoxine Hydrochloride, Niacinamide, Dexpanthenol, Alpha-tocopherol acetate, Vitamin K, Folic Acid, Biotin and 1 more
Dosage form KIT
Route INTRAVENOUS
Labeler Apotex Corp.
Product type HUMAN PRESCRIPTION DRUG
Marketing category ANDA
Application number ANDA210672
Marketing start Jun 4, 2026
Listing certified through Dec 31, 2027

At a glance

  • 1–9 Package NDCs

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The National Drug Code (NDC) is the FDA's product identifier for drugs; the product NDC identifies the labeler and product, and each package adds a package code.

Source: U.S. Food and Drug Administration (FDA), National Drug Code Directory · Source date:

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