United States · FDA National Drug Code directory
ETHAMBUTOL HYDROCHLORIDE
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
- 10135-796_2dcb6b41-b9a8-4dde-8248-334d13f87a29
- Product NDC
- 10135-796
- Form
- TABLET, FILM COATED
- Composition / generic term
- ETHAMBUTOL HYDROCHLORIDE
- Labeler
- Marlex Pharmaceuticals, Inc.
- Marketing category
- NDA
- Marketing start / end (source format)
- 20061215
- Source listing expiry
- 20261231
Source-listed ingredients
- ETHAMBUTOL HYDROCHLORIDE — 100 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET, FILM COATED in 1 BOTTLE (10135-796-01) · 10135-796-01
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.
Browse United States records →