United States · FDA National Drug Code directory

CARBINOXAMINE MALEATE

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
69315-239_a6ac5a29-dc4e-425f-bcaf-d362b08e887c
Product NDC
69315-239
Form
TABLET
Composition / generic term
CARBINOXAMINE MALEATE
Labeler
Leading Pharma, LLC
Marketing category
ANDA
Marketing start / end (source format)
20250801
Source listing expiry
20261231

Source-listed ingredients

  • CARBINOXAMINE MALEATE — 6 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 100 TABLET in 1 BOTTLE (69315-239-01) · 69315-239-01

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 →