United States · FDA National Drug Code directory
Amoxicillin
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
- 71205-817_2c395111-c9c1-483e-a542-58b935ede689
- Product NDC
- 71205-817
- Form
- CAPSULE
- Composition / generic term
- Amoxicillin
- Labeler
- Proficient Rx LP
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20051109
- Source listing expiry
- 20261231
Source-listed ingredients
- AMOXICILLIN — 500 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 14 CAPSULE in 1 BOTTLE (71205-817-14) · 71205-817-14
- 20 CAPSULE in 1 BOTTLE (71205-817-20) · 71205-817-20
- 21 CAPSULE in 1 BOTTLE (71205-817-21) · 71205-817-21
- 30 CAPSULE in 1 BOTTLE (71205-817-30) · 71205-817-30
- 40 CAPSULE in 1 BOTTLE (71205-817-40) · 71205-817-40
- 60 CAPSULE in 1 BOTTLE (71205-817-60) · 71205-817-60
- 90 CAPSULE in 1 BOTTLE (71205-817-90) · 71205-817-90
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 →