United States · FDA National Drug Code directory

Bepotastine Besilate

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
0378-7055_c8ce95fa-e800-433e-8d40-70a6b1e06140
Product NDC
0378-7055
Form
SOLUTION/ DROPS
Composition / generic term
Bepotastine Besilate
Labeler
Mylan Pharmaceuticals Inc.
Marketing category
ANDA
Marketing start / end (source format)
20210528
Source listing expiry
20261231

Source-listed ingredients

  • BEPOTASTINE BESILATE — 15 mg/mL

These values do not establish equivalence or a dose recommendation.

Packages

  • 1 BOTTLE, DROPPER in 1 CARTON (0378-7055-35) / 5 mL in 1 BOTTLE, DROPPER · 0378-7055-35
  • 1 BOTTLE, DROPPER in 1 CARTON (0378-7055-67) / 10 mL in 1 BOTTLE, DROPPER · 0378-7055-67

Source and coverage

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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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