United States · FDA National Drug Code directory

CARBAMAZEPINE

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
62332-731_a2eb2307-49f2-44de-9398-7a4783a26851
Product NDC
62332-731
Form
TABLET
Composition / generic term
CARBAMAZEPINE
Labeler
Alembic Pharmaceuticals Inc.
Marketing category
ANDA
Marketing start / end (source format)
20241231
Source listing expiry
20271231

Source-listed ingredients

  • CARBAMAZEPINE — 200 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 100 BLISTER PACK in 1 CARTON (62332-731-10) / 10 TABLET in 1 BLISTER PACK · 62332-731-10
  • 100 TABLET in 1 BOTTLE (62332-731-31) · 62332-731-31
  • 60 TABLET in 1 BOTTLE (62332-731-60) · 62332-731-60
  • 1000 TABLET in 1 BOTTLE (62332-731-91) · 62332-731-91

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 →
CARBAMAZEPINE — United States | Molindra Medicines