NDC product

Topiramate

NDC 70771-1675 · Zydus Lifesciences Limited

Key facts

Product NDC 70771-1675
Proprietary name Topiramate
Labeler Zydus Lifesciences Limited
Marketing category ANDA
Application number ANDA216167
Marketing start Aug 9, 2026
Listing certified through Dec 31, 2024

At a glance

  • 1–9 Package NDCs

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About National Drug Codes (NDC)

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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