United States · FDA National Drug Code directory

Dichlorphenamide

A source-listed medicine record.

Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.

Medicine identity

Source reference
13668-676_1d0520f1-bf08-4def-a715-2ab45a18393e
Product NDC
13668-676
Form
TABLET
Composition / generic term
Dichlorphenamide
Labeler
Torrent pharmaceuticals limited
Marketing category
ANDA
Marketing start / end (source format)
20221229
Source listing expiry
20271231

Source-listed ingredients

  • DICHLORPHENAMIDE — 50 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 100 TABLET in 1 BOTTLE (13668-676-01) · 13668-676-01
  • 30 TABLET in 1 BOTTLE (13668-676-30) · 13668-676-30

Source and coverage

Open FDA National Drug Code directory

Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.

Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.

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