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
- 59651-322_1a37b4f8-8f1f-4aed-9409-6c22716c5b68
- Product NDC
- 59651-322
- Form
- POWDER, FOR SUSPENSION
- Composition / generic term
- Cephalexin
- Labeler
- Aurobindo Pharma Limited
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20260609
- Source listing expiry
- 20271231
Source-listed ingredients
- CEPHALEXIN — 125 mg/5mL
These values do not establish equivalence or a dose recommendation.
Packages
- 100 mL in 1 BOTTLE (59651-322-01) · 59651-322-01
- 200 mL in 1 BOTTLE (59651-322-02) · 59651-322-02
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 →