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
- 71205-672_c69d7a12-1f34-4acc-966c-c4adf3cd84db
- Product NDC
- 71205-672
- Form
- CAPSULE
- Composition / generic term
- Cephalexin
- Labeler
- Proficient Rx LP
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20110119
- Source listing expiry
- 20271231
Source-listed ingredients
- CEPHALEXIN — 500 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 6 CAPSULE in 1 BOTTLE (71205-672-06) · 71205-672-06
- 14 CAPSULE in 1 BOTTLE (71205-672-14) · 71205-672-14
- 15 CAPSULE in 1 BOTTLE (71205-672-15) · 71205-672-15
- 20 CAPSULE in 1 BOTTLE (71205-672-20) · 71205-672-20
- 21 CAPSULE in 1 BOTTLE (71205-672-21) · 71205-672-21
- 28 CAPSULE in 1 BOTTLE (71205-672-28) · 71205-672-28
- 30 CAPSULE in 1 BOTTLE (71205-672-30) · 71205-672-30
- 40 CAPSULE in 1 BOTTLE (71205-672-40) · 71205-672-40
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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