United States · FDA National Drug Code directory

Cephalexin

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
69778-930_5f2379e6-9041-4de6-83a2-f63fa36db0d9
Product NDC
69778-930
Form
CAPSULE
Composition / generic term
Cephalexin
Labeler
Pharma-C, Inc.
Marketing category
ANDA
Marketing start / end (source format)
20101015
Source listing expiry
20261231

Source-listed ingredients

  • CEPHALEXIN — 250 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 500 CAPSULE in 1 BOTTLE, PLASTIC (69778-930-04) · 69778-930-04

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 →