NDC product

CLARITHROMYCIN

NDC 62135-615 · Chartwell RX, LLC.

Key facts

Product NDC 62135-615
Proprietary name CLARITHROMYCIN
Nonproprietary name Clarithromycin
Substances CLARITHROMYCIN
Dosage form TABLET, FILM COATED
Route ORAL
Labeler Chartwell RX, LLC.
Product type HUMAN PRESCRIPTION DRUG
Marketing category ANDA
Application number ANDA065384
Pharmacologic classes Cytochrome P450 3A Inhibitors [MoA], Cytochrome P450 3A4 Inhibitors [MoA], Macrolide Antimicrobial [EPC], Macrolides [CS], P-Glycoprotein Inhibitors [MoA]
Marketing start Aug 20, 2007
Listing certified through Dec 31, 2026

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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