United States · FDA National Drug Code directory

MYTESI

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
70564-802_f9b7d7cd-31ef-4030-ae3f-10ab635d0758
Product NDC
70564-802
Form
TABLET, COATED
Composition / generic term
Crofelemer
Labeler
Napo Pharmaceuticals, Inc.
Marketing category
NDA
Marketing start / end (source format)
20160801
Source listing expiry
20271231

Source-listed ingredients

  • CROFELEMER — 125 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 60 TABLET, COATED in 1 BOTTLE (70564-802-60) · 70564-802-60
  • 60 TABLET, COATED in 1 BOTTLE (70564-802-99) · 70564-802-99

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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